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Salmonella enterica subsp. enterica serovar Heidelberg str. SL476 (sent8)
Gene : ACF66668.1
DDBJ      :             ferrichrome transport system permease protein FhuB
Swiss-Prot:FHUB_SALTY   RecName: Full=Iron(3+)-hydroxamate import system permease protein fhuB;AltName: Full=Iron(III)-hydroxamate import system permease protein fhuB;AltName: Full=Ferrichrome transport system permease protein fhuB;AltName: Full=Ferrichrome uptake protein fhuB;AltName: Full=Ferric hydroxamate uptake protein B;

Homologs  Archaea  37/68 : Bacteria  540/915 : Eukaryota  1/199 : Viruses  0/175   --->[See Alignment]
f.22.1
:685 amino acids
:SECSTR
:PSIPRED
:DISOPRED
:BLT:PDB   436->682 1l7vA PDBj 3e-13 29.3 %
:RPS:SCOP  67->341 1l7vA  f.22.1.1 * 5e-17 22.7 %
:RPS:SCOP  406->682 1l7vA  f.22.1.1 * 8e-42 28.6 %
:HMM:SCOP  20->350 1l7vA_ f.22.1.1 * 2.9e-57 37.8 %
:HMM:SCOP  360->683 1l7vA_ f.22.1.1 * 8.3e-70 36.8 %
:RPS:PFM   109->341 PF01032 * FecCD 5e-10 30.8 %
:RPS:PFM   405->682 PF01032 * FecCD 4e-32 38.5 %
:HMM:PFM   43->349 PF01032 * FecCD 9e-73 39.3 305/311  
:HMM:PFM   408->682 PF01032 * FecCD 2e-76 41.1 275/311  
:HMM:PFM   21->32 PF12035 * DUF3521 0.00094 66.7 12/35  
:BLT:SWISS 1->685 FHUB_SALTY 0.0 98.8 %
:TM
:SEG

SeqInfo AminoSeq See neighboring genes
Links DAD Abbreviations Back to title page
GT:ID ACF66668.1 GT:GENE ACF66668.1 GT:PRODUCT ferrichrome transport system permease protein FhuB GT:DATABASE GIB00763CH01 GT:ORG sent8 GB:ACCESSION GIB00763CH01 GB:LOCATION 235398..237455 GB:FROM 235398 GB:TO 237455 GB:DIRECTION + GB:PRODUCT ferrichrome transport system permease protein FhuB GB:NOTE identified by match to protein family HMM PF01032; match to protein family HMM TIGR01409 GB:PROTEIN_ID ACF66668.1 GB:DB_XREF GI:194406449 LENGTH 685 SQ:AASEQ MSRKREMPDGGAKSALSDLRFGRFVGRIRRSRHPALLLLALFVAACWLTWVNFSVALPRSQWQQAIWSPDIDIIEQMIFHYSLLPRLAISLLVGAGLGLVGVLFQQVLRNPLAEPTTLGVATGAQLGITVTTLWAIPGALATQFAALTGACIVGALVFGVAWGKRLSPVTLILAGLVVSLYCGAINQLLVIFHHDQLQSMFLWSTGTLTQTDWSGVQRLWPQLLGGVMLTLLLLRPMTLMGLDDGVARNLGLALSLARLAALSLAIVLSALLVNAVGIIGFIGLFAPLLAKMLGARRLLARLMLAPLIGALILWLSDQIILWLTRVWMEVSTGSVTALIGAPLLLWLLPRLKSMSAPDMNASDRVAAERRHVLAFAVAGGALLLLATWGALSFGRDAHGWTWASGTLLEELMPWRWPRILAALMAGVMLAVAGCIIQRLTGNPMASPEVLGISSGAAFGLVLMLFLVPGNAFGWLLPAGSLGAAATLLIIMLAAGRGGFSPQRMLLAGMALSTAFTMLLMMLQASGDPRMAEVLTWIAGSTYNATGGQVTRTAIVMVILLAIVPLCRRWLTILPLGGDAARAVGMALTPSRIALLALAACLTATATMTIGPLSFVGLMAPHIARMLGFRRTMPHMVISALAGGVLLVFADWCGRMALFPYQIPAGLLSSFIGAPYFIYLLRKQSR GT:EXON 1|1-685:0| SW:ID FHUB_SALTY SW:DE RecName: Full=Iron(3+)-hydroxamate import system permease protein fhuB;AltName: Full=Iron(III)-hydroxamate import system permease protein fhuB;AltName: Full=Ferrichrome transport system permease protein fhuB;AltName: Full=Ferrichrome uptake protein fhuB;AltName: Full=Ferric hydroxamate uptake protein B; SW:GN Name=fhuB; OrderedLocusNames=STM0194; SW:KW Cell inner membrane; Cell membrane; Complete proteome; Ion transport;Iron; Iron transport; Membrane; Transmembrane; Transport. SW:EXACT F SW:FUNC + BL:SWS:NREP 1 BL:SWS:REP 1->685|FHUB_SALTY|0.0|98.8|685/685| GO:SWS:NREP 7 GO:SWS GO:0005886|"GO:plasma membrane"|Cell inner membrane| GO:SWS GO:0005886|"GO:plasma membrane"|Cell membrane| GO:SWS GO:0006811|"GO:ion transport"|Ion transport| GO:SWS GO:0006826|"GO:iron ion transport"|Iron transport| GO:SWS GO:0016020|"GO:membrane"|Membrane| GO:SWS GO:0016021|"GO:integral to membrane"|Transmembrane| GO:SWS GO:0006810|"GO:transport"|Transport| TM:NTM 18 TM:REGION 35->57| TM:REGION 77->99| TM:REGION 130->152| TM:REGION 176->198| TM:REGION 219->241| TM:REGION 245->267| TM:REGION 273->295| TM:REGION 302->324| TM:REGION 329->350| TM:REGION 371->393| TM:REGION 418->440| TM:REGION 445->467| TM:REGION 474->496| TM:REGION 503->525| TM:REGION 547->566| TM:REGION 591->613| TM:REGION 631->653| TM:REGION 660->681| SEG 35->48|allllalfvaacwl| SEG 91->108|llvgaglglvgvlfqqvl| SEG 223->242|llggvmltllllrpmtlmgl| SEG 247->276|arnlglalslarlaalslaivlsallvnav| SEG 288->307|llakmlgarrllarlmlapl| SEG 342->351|plllwllprl| SEG 373->391|lafavaggallllatwgal| SEG 420->433|laalmagvmlavag| SEG 481->495|lgaaatlliimlaag| SEG 593->608|allalaacltatatmt| BL:PDB:NREP 1 BL:PDB:REP 436->682|1l7vA|3e-13|29.3|239/313| RP:PFM:NREP 2 RP:PFM:REP 109->341|PF01032|5e-10|30.8|231/313|FecCD| RP:PFM:REP 405->682|PF01032|4e-32|38.5|275/313|FecCD| HM:PFM:NREP 3 HM:PFM:REP 43->349|PF01032|9e-73|39.3|305/311|FecCD| HM:PFM:REP 408->682|PF01032|2e-76|41.1|275/311|FecCD| HM:PFM:REP 21->32|PF12035|0.00094|66.7|12/35|DUF3521| GO:PFM:NREP 6 GO:PFM GO:0005215|"GO:transporter activity"|PF01032|IPR000522| GO:PFM GO:0006810|"GO:transport"|PF01032|IPR000522| GO:PFM GO:0016020|"GO:membrane"|PF01032|IPR000522| GO:PFM GO:0005215|"GO:transporter activity"|PF01032|IPR000522| GO:PFM GO:0006810|"GO:transport"|PF01032|IPR000522| GO:PFM GO:0016020|"GO:membrane"|PF01032|IPR000522| RP:SCP:NREP 2 RP:SCP:REP 67->341|1l7vA|5e-17|22.7|268/324|f.22.1.1| RP:SCP:REP 406->682|1l7vA|8e-42|28.6|276/324|f.22.1.1| HM:SCP:REP 20->350|1l7vA_|2.9e-57|37.8|320/324|f.22.1.1|1/2|ABC transporter involved in vitamin B12 uptake, BtuC| HM:SCP:REP 360->683|1l7vA_|8.3e-70|36.8|323/324|f.22.1.1|2/2|ABC transporter involved in vitamin B12 uptake, BtuC| OP:NHOMO 1758 OP:NHOMOORG 578 OP:PATTERN --1------------------111211212211--11-112111163653B71-2222222------- -----4337794621----------2----------2935-312-2-1222-62--131111-654224A3---------221-----111---11-----1111-121----------------12111--1122-22111126-5-2222-----------32--441-------------111--22-166BBCBCABB5CBCCCB879998CCC4768643222222FF255555555555555422552-1--------33-1--2-----11111122321--111111111112222222222222211---11122392266665765951222254425---32--2971--111111122-4-21-1---1----21---11122111----------3-11-111-121--4664441354553112-1151-112--11111111-111--------------------------------------2-1112-3324111111--1-111111211---1--111-11111-1---1-1-1-121---------1-11-4322-121-311-----1---23------33-243-11112----------11---11232131112--1122-1121112-122222---11-1------C3661754666466643-5453667364576444443778776454343444444544434633644441-555555545555--1-----------1539222131---1-1--5--11-11-213--1--211521111-456---------15332333338481111----------------11------------2--------------------------11121122222--- --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------1---------- ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- STR:NPRED 268 STR:RPRED 39.1 SQ:SECSTR ##############################################################################################################################################################################################################################################################################################################################################################################################################################HHHHHHHHHHHHHHHHHHHHHHHHHHTcTTccTTTTTHHHHHHHHHHHHHHTccTTccHHHHHHHHHHHHHHHHHHHHHHHHHTccHHHHHHHHHHHHHHHHHHHHHHHHHccccHHHHHHHTTcccHcccTTccGGGHHHHHHHHHHHHHHHcHHHHHHHcHHHHHHTTccHHHHHHHHHHHHHHHHHHHHHHHccccccccHHHHHHHHTTcccHHHHHHHHHHHHHHHHHHHHHHHHHccccccccHHHHHHHHHHHHHHHHHHc### DISOP:02AL 1-14,350-371| PSIPRED ccccccccccHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHccccccHHHHHHHHccccccHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHccccccccHHHHHHHHHHHHHHHHHHccccHHHHHHHHHHHHHHHHHHHHHHccccccccHHHHHHHHHHHHHHHHHHHHHHHHcHHHHHHHHHHHccccccccHHHHHHHHHHHHHHHHHHHHHccccccccccHHHHHHccccHHHHHHHHHHHHHHHHHHHHHHHcHHHHHHHHHHHHHHHHHcccccHHHHHHHHHHHHHHHHHHHHHHHHHcccccccHHHHHHHHHHHHHHHHHHHHHHccccccccHHcccccccccHHHHHHHHHHHHHHHHHHHHHHccccccccccHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHccccccccHHHHccHHHHHHHHHHHHccccHHHHHHHHHHHHHHHHHHHHHHHHccccccHHHHHHHHHHHHHHHHHHHHHHHHHccHHHHHHHHHHccccccccHHHHHHHHHHHHHHHHHHHHHcccccEEcccHHHHHHccccHHHHHHHHHHHHHHHHHHHHHHHcHHHHHHHHHHHHHHHHHccccccHHHHHHHHHHHHHHHHHHHHHHHcccccccHHHHHHHHHHHHHHHHHHHccc //