GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatA in Klebsiella michiganensis M5al

Align Inositol transport ATP-binding protein IatA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate BWI76_RS07240 BWI76_RS07240 D-ribose transporter ATP-binding protein

Query= TCDB::B8H229
         (515 letters)



>FitnessBrowser__Koxy:BWI76_RS07240
          Length = 494

 Score =  374 bits (959), Expect = e-108
 Identities = 210/494 (42%), Positives = 307/494 (62%), Gaps = 10/494 (2%)

Query: 4   LDVSQVSKSFPGVRALDQVDLVVGVGEVHALLGENGAGKSTLIKILSAAHAADAGTVTFA 63
           L+   +SK FPGV+ALD V L V  G VHAL+GENGAGKSTL+K L   +  D G +   
Sbjct: 6   LEAEGISKFFPGVKALDNVSLRVRPGTVHALMGENGAGKSTLMKCLIGIYRPDKGAIRVK 65

Query: 64  GQVLDPRDAPLRRQQLGIATIYQEFNLFPELSVAENMYLGREPRRLGLVDWSRLRADAQA 123
           G+ +  +D  +   + GI+ I+QE NL P ++VAEN++LGREP + G VD  +L    Q 
Sbjct: 66  GEPVQFQDT-MDALRSGISMIHQELNLVPHMTVAENIWLGREPMKYGFVDHRQLARQTQD 124

Query: 124 LLNDLGLPLNPDAPVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREVDRLHAII 183
           LL+ L + L+ D  V  L++A QQMVEIAKA++ NA ++IMDEPT+AL+  EV  L  II
Sbjct: 125 LLDKLNIRLSADRLVGELSIASQQMVEIAKAVSWNADIVIMDEPTSALTESEVAHLFTII 184

Query: 184 AGLKARSVSVIYVSHRLGEVKAMCDRYTVMRDGRFVASGDVADVEVADMVRLMVGRHVEF 243
             L+ +  ++IY+SH++ E+ A+ D  +V RDG +V S    +     ++  MVGR +  
Sbjct: 185 RDLRQQGKAIIYISHKMDEIFAITDEISVFRDGTWVGSKQTTEFTRQSLITQMVGRELTQ 244

Query: 244 ERRKRRRPPGAVVLKVEGVTPAAPRLSAPGYLRQVSFAARGGEIVGLAGLVGAGRTDLAR 303
              K     G  VL V         LS  G    ++F+ R GEI+G+AGLVGAGR+++  
Sbjct: 245 LFPKFNNAIGEEVLTVR-------NLSRKGAFHDINFSVRRGEILGVAGLVGAGRSEVME 297

Query: 304 LIFGADPIAAGRVLVDDKPLRLRSPRDAIQAGIMLVPEDRKQQGCFLDHSIRRNLSLPSL 363
            +FG +   +G VL+D  P+ + SP  AI+ G+ L+ EDRK+ G FL  S+  N+S+  +
Sbjct: 298 SLFGMEKADSGEVLIDGMPVNIDSPSTAIEKGMALLTEDRKKSGLFLVLSVLENMSIVKM 357

Query: 364 KALSALGQWVDE-RAERDLVETYRQKLRIKMADAETAIGKLSGGNQQKVLLGRAMALTPK 422
                   +V   +   D +E  R +L IK    +  I  LSGGNQQKVL+ R +   PK
Sbjct: 358 PEYIGKTGFVQHLKMAEDCMEQIR-RLNIKTPTMDQIINNLSGGNQQKVLIARWLLAQPK 416

Query: 423 VLIVDEPTRGIDIGAKAEVHQVLSDLADLGVAVVVISSELAEVMAVSDRIVVFREGVIVA 482
           +LI+DEPTRGID+GAKAE++ ++S+LA+ GVAV+++SSEL E++ +SDR++V  EG I  
Sbjct: 417 ILILDEPTRGIDVGAKAEIYHLISELANRGVAVIMVSSELPEILGMSDRVMVMHEGRITG 476

Query: 483 DLDAQTATEEGLMA 496
            LD + A +E +++
Sbjct: 477 ILDKEDADQETILS 490



 Score = 92.8 bits (229), Expect = 3e-23
 Identities = 66/246 (26%), Positives = 121/246 (49%), Gaps = 12/246 (4%)

Query: 254 AVVLKVEGVTPAAPRLSAPGYLRQVSFAARGGEIVGLAGLVGAGRTDLARLIFGADPIAA 313
           A  L+ EG++   P + A   L  VS   R G +  L G  GAG++ L + + G      
Sbjct: 3   AFALEAEGISKFFPGVKA---LDNVSLRVRPGTVHALMGENGAGKSTLMKCLIGIYRPDK 59

Query: 314 GRVLVDDKPLRLRSPRDAIQAGIMLVPEDRKQQGCFLDH-SIRRNLSLPSLKALSALGQW 372
           G + V  +P++ +   DA+++GI ++ ++       + H ++  N+ L           +
Sbjct: 60  GAIRVKGEPVQFQDTMDALRSGISMIHQELN----LVPHMTVAENIWLGREPMKYG---F 112

Query: 373 VDERAERDLVETYRQKLRIKMADAETAIGKLSGGNQQKVLLGRAMALTPKVLIVDEPTRG 432
           VD R      +    KL I+++ A+  +G+LS  +QQ V + +A++    ++I+DEPT  
Sbjct: 113 VDHRQLARQTQDLLDKLNIRLS-ADRLVGELSIASQQMVEIAKAVSWNADIVIMDEPTSA 171

Query: 433 IDIGAKAEVHQVLSDLADLGVAVVVISSELAEVMAVSDRIVVFREGVIVADLDAQTATEE 492
           +     A +  ++ DL   G A++ IS ++ E+ A++D I VFR+G  V        T +
Sbjct: 172 LTESEVAHLFTIIRDLRQQGKAIIYISHKMDEIFAITDEISVFRDGTWVGSKQTTEFTRQ 231

Query: 493 GLMAYM 498
            L+  M
Sbjct: 232 SLITQM 237



 Score = 83.2 bits (204), Expect = 2e-20
 Identities = 64/225 (28%), Positives = 107/225 (47%), Gaps = 8/225 (3%)

Query: 18  ALDQVDLVVGVGEVHALLGENGAGKSTLIKILSAAHAADAGTVTFAGQVLDPRDAPLRRQ 77
           A   ++  V  GE+  + G  GAG+S +++ L     AD+G V   G  ++  D+P    
Sbjct: 268 AFHDINFSVRRGEILGVAGLVGAGRSEVMESLFGMEKADSGEVLIDGMPVNI-DSPSTAI 326

Query: 78  QLGIATIYQE---FNLFPELSVAENMYLGREPR---RLGLVDWSRLRADAQALLNDLGLP 131
           + G+A + ++     LF  LSV ENM + + P    + G V   ++  D    +  L + 
Sbjct: 327 EKGMALLTEDRKKSGLFLVLSVLENMSIVKMPEYIGKTGFVQHLKMAEDCMEQIRRLNIK 386

Query: 132 L-NPDAPVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREVDRLHAIIAGLKARS 190
               D  +  L+   QQ V IA+ +    +++I+DEPT  +       ++ +I+ L  R 
Sbjct: 387 TPTMDQIINNLSGGNQQKVLIARWLLAQPKILILDEPTRGIDVGAKAEIYHLISELANRG 446

Query: 191 VSVIYVSHRLGEVKAMCDRYTVMRDGRFVASGDVADVEVADMVRL 235
           V+VI VS  L E+  M DR  VM +GR     D  D +   ++ L
Sbjct: 447 VAVIMVSSELPEILGMSDRVMVMHEGRITGILDKEDADQETILSL 491


Lambda     K      H
   0.320    0.136    0.380 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 609
Number of extensions: 36
Number of successful extensions: 9
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 3
Length of query: 515
Length of database: 494
Length adjustment: 34
Effective length of query: 481
Effective length of database: 460
Effective search space:   221260
Effective search space used:   221260
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory