GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nupA in Trichormus variabilis ATCC 29413

Align Purine/cytidine ABC transporter ATP-binding protein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized)
to candidate WP_011318959.1 AVA_RS10980 sugar ABC transporter ATP-binding protein

Query= TCDB::A2RKA7
         (506 letters)



>NCBI__GCF_000204075.1:WP_011318959.1
          Length = 517

 Score =  328 bits (841), Expect = 3e-94
 Identities = 184/479 (38%), Positives = 290/479 (60%), Gaps = 8/479 (1%)

Query: 6   VIQMIDVTKRFGDFVANDKVNLELKKGEIHALLGENGAGKSTLMNILSGLLEPSEGEVHV 65
           V++M  + KRF    A   VNL +  GE+HAL+GENGAGKSTLM IL+G     EGE+ +
Sbjct: 18  VLEMQGIAKRFHGVPALQGVNLTIYPGEVHALMGENGAGKSTLMKILAGAYIADEGEIRI 77

Query: 66  KGKLENIDSPSKAANLGIGMVHQHFMLVDAFTVTENIILGNEVTKGINLDLKTAKKKILE 125
            GK   I  P  A   GI +++Q   +    TVTENI +G+E+T+G  LD K  + +  +
Sbjct: 78  NGKGVKITDPGTARQAGINLIYQELNVAPNLTVTENIFMGSELTRGQFLDRKAMELEAQQ 137

Query: 126 LSERYGLSVEPDALIRDISVGQQQRVEILKTLYRGADILIFDEPTAVLTPAEITELMQIM 185
           +    G S  P  ++  +++ +QQ+VEI + L   + IL+ DEPTA L+  E   L +++
Sbjct: 138 VLASLGASFAPTDIVGTLAIAEQQQVEIARALKDNSRILVMDEPTAALSDRETERLFEVI 197

Query: 186 KNLIKEGKSIILITHKLDEIRAVADRITVIRRGKSIDTVELGDKTNQELAELMVGRSV-S 244
           + L  +G +II I+H+++EI A+ADRI+V+R G+ I ++   + + Q L ++MVGRS+  
Sbjct: 198 RKLRNDGIAIIYISHRMEEIYALADRISVLRDGQYIGSLTREEISPQRLVQMMVGRSMQD 257

Query: 245 FITEKAAAQPKDVVLEIKDLNIKESRGSLKVKGLSLDVRAGEIVGVAGIDGNGQTELVKA 304
           F   +  + P  VVLE++  NI + R   KV+  S  +RAGEI+G+AG+ G G+TE+ + 
Sbjct: 258 FYEHQRQSNPGPVVLEVR--NISDGR---KVQPASFQLRAGEILGLAGLVGAGRTEVSRL 312

Query: 305 ITGLTKVDSGSIKLHNKDITNQRPRKITEQSVGHVPEDRHRDGLVLEMTVAENIALQTYY 364
           I G  +  SG + L+ K +    P       +G+VPEDR   GL LEM+  +NI L    
Sbjct: 313 IFGADRKVSGEVFLNGKKLEIHSPSDAIAVGIGYVPEDRKDQGLFLEMSSRKNIGLNRLK 372

Query: 365 KPPMSKYGFLDYNKINSHARELMEEFDVRGAGEWVSASSLSGGNQQKAIIAREIDRNPDL 424
           +   +  G +++  +N  A + +E F +R A   + A  LSGGNQQK ++AR +  NP +
Sbjct: 373 QD--ANLGIVNWGSVNKIATDAVENFHIRLANLEIRAVDLSGGNQQKLLLARWLAINPRV 430

Query: 425 LIVSQPTRGLDVGAIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHDGQIQG 483
           L++ +PTRG+D+GA   I++ +     +G A+L++S EL EI+ +SDR+ V+ +GQ+ G
Sbjct: 431 LMLDEPTRGVDIGAKSEIYRIISDLSAQGVAILMVSSELPEIVGLSDRVLVMREGQLVG 489



 Score = 92.0 bits (227), Expect = 4e-23
 Identities = 63/249 (25%), Positives = 130/249 (52%), Gaps = 9/249 (3%)

Query: 258 VLEIKDLNIKESRGSLKVKGLSLDVRAGEIVGVAGIDGNGQTELVKAITGLTKVDSGSIK 317
           VLE++ +  K   G   ++G++L +  GE+  + G +G G++ L+K + G    D G I+
Sbjct: 18  VLEMQGI-AKRFHGVPALQGVNLTIYPGEVHALMGENGAGKSTLMKILAGAYIADEGEIR 76

Query: 318 LHNKDITNQRPRKITEQSVGHVPEDRHRDGLVLEMTVAENIALQTYYKPPMSKYGFLDYN 377
           ++ K +    P    +  +  + ++ +   +   +TV ENI + +     +++  FLD  
Sbjct: 77  INGKGVKITDPGTARQAGINLIYQELN---VAPNLTVTENIFMGS----ELTRGQFLDRK 129

Query: 378 KINSHARELMEEFDVRGAGEWVSASSLSGGNQQKAIIAREIDRNPDLLIVSQPTRGLDVG 437
            +   A++++       A   +   +L+   QQ+  IAR +  N  +L++ +PT  L   
Sbjct: 130 AMELEAQQVLASLGASFAPTDI-VGTLAIAEQQQVEIARALKDNSRILVMDEPTAALSDR 188

Query: 438 AIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHDGQIQGIVSPETTTKQELGI 497
             E + + + + R++G A++ IS  ++EI  ++DRI+V+ DGQ  G ++ E  + Q L  
Sbjct: 189 ETERLFEVIRKLRNDGIAIIYISHRMEEIYALADRISVLRDGQYIGSLTREEISPQRLVQ 248

Query: 498 LMVGGNINE 506
           +MVG ++ +
Sbjct: 249 MMVGRSMQD 257



 Score = 76.6 bits (187), Expect = 2e-18
 Identities = 60/217 (27%), Positives = 112/217 (51%), Gaps = 10/217 (4%)

Query: 26  NLELKKGEIHALLGENGAGKSTLMNILSGLLEPSEGEVHVKGKLENIDSPSKAANLGIGM 85
           + +L+ GEI  L G  GAG++ +  ++ G      GEV + GK   I SPS A  +GIG 
Sbjct: 287 SFQLRAGEILGLAGLVGAGRTEVSRLIFGADRKVSGEVFLNGKKLEIHSPSDAIAVGIGY 346

Query: 86  VHQHFMLVDAF---TVTENIILGNEVTKGINLDLK---TAKKKILELSERYGLSVEP-DA 138
           V +       F   +  +NI L N + +  NL +    +  K   +  E + + +   + 
Sbjct: 347 VPEDRKDQGLFLEMSSRKNIGL-NRLKQDANLGIVNWGSVNKIATDAVENFHIRLANLEI 405

Query: 139 LIRDISVGQQQRVEILKTLYRGADILIFDEPTAVLTPAEITELMQIMKNLIKEGKSIILI 198
              D+S G QQ++ + + L     +L+ DEPT  +     +E+ +I+ +L  +G +I+++
Sbjct: 406 RAVDLSGGNQQKLLLARWLAINPRVLMLDEPTRGVDIGAKSEIYRIISDLSAQGVAILMV 465

Query: 199 THKLDEIRAVADRITVIRRGKSIDTVE--LGDKTNQE 233
           + +L EI  ++DR+ V+R G+ +  ++  +G +  QE
Sbjct: 466 SSELPEIVGLSDRVLVMREGQLVGELDNSIGKEITQE 502


Lambda     K      H
   0.315    0.135    0.365 

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: 660
Number of extensions: 28
Number of successful extensions: 7
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: 506
Length of database: 517
Length adjustment: 35
Effective length of query: 471
Effective length of database: 482
Effective search space:   227022
Effective search space used:   227022
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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