Alignments for a candidate for nupA in Pseudovibrio axinellae Ad2

GapMind for catabolism of small carbon sources

Alignments for a candidate for nupA in Pseudovibrio axinellae Ad2

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_068000812.1 PsAD2_RS00245 ABC transporter ATP-binding protein

Query= TCDB::A2RKA7
         (506 letters)



>NCBI__GCF_001623255.1:WP_068000812.1
          Length = 514

 Score =  456 bits (1173), Expect = e-133
 Identities = 235/505 (46%), Positives = 344/505 (68%), Gaps = 4/505 (0%)

Query: 2   ANETVIQMIDVTKRFGDFVANDKVNLELKKGEIHALLGENGAGKSTLMNILSGLLEPSEG 61
           +N   I++I V K FG   AN  ++L + KG IH ++GENGAGKSTLM+IL G      G
Sbjct: 4   SNVPAIELIGVNKSFGPVHANKDIDLVVGKGSIHGIIGENGAGKSTLMSILYGFYHADSG 63

Query: 62  EVHVKGKLENIDSPSKAANLGIGMVHQHFMLVDAFTVTENIILGNEVTKGINLDLKTAKK 121
            + + GK   I     A + GIGMVHQHFMLVD FTV EN++LG E    +   +  A++
Sbjct: 64  TIKIDGKATTIPDSKSAISQGIGMVHQHFMLVDPFTVLENVVLGAEGGALLKDGVANARR 123

Query: 122 KILELSERYGLSVEPDALIRDISVGQQQRVEILKTLYRGADILIFDEPTAVLTPAEITEL 181
           ++  L++ Y ++++PDA++ ++ VG QQRVEILK LYRGADILI DEPT VLTP+E   L
Sbjct: 124 ELKRLADEYDMTIDPDAVVGELPVGLQQRVEILKALYRGADILILDEPTGVLTPSEADHL 183

Query: 182 MQIMKNLIKEGKSIILITHKLDEIRAVADRITVIRRGKSIDTVELGDKTNQELAELMVGR 241
            +I++ L  +GK+++LITHKL EI  V D ++V+RRG+ + + +    + +ELAELMVGR
Sbjct: 184 FRILRVLRDQGKTVLLITHKLREIMDVTDTVSVMRRGEMVASRKTAQTSMEELAELMVGR 243

Query: 242 SVSFITEKAAAQPKDVVLEIKDLNIKESRGSLKVKGLSLDVRAGEIVGVAGIDGNGQTEL 301
           SV     K   +    +L+++ LN+K+ RG  +VK +S +VRAGE++G+AG+ GNGQ+EL
Sbjct: 244 SVLLEVSKPDVEVGKPLLKVEGLNVKDERGVRRVKDVSFEVRAGEVLGIAGVSGNGQSEL 303

Query: 302 VKAITGLTKVDSGSIKLHNKDITNQR---PRKITEQSVGHVPEDRHRDGLVLEMTVAENI 358
           + A+ G+T+ +SGS++L  + +         ++ ++ + HVPEDRHR GLV + + AEN 
Sbjct: 304 MAALAGITRAESGSMELAGQKLDLSEVHDAAQMRDRGMSHVPEDRHRMGLVNKFSEAENS 363

Query: 359 ALQTYYKPPMSKYGFLDYNKINSHARELMEEFDVRGAGEWVSASSLSGGNQQKAIIAREI 418
            L  + +   SK  FLD + I   A+E +E++D+R     ++A+  SGGNQQK ++AREI
Sbjct: 364 ILGYHRESKYSKGMFLDKDAIRKEAKERIEKYDIRPPLTEMTAAKFSGGNQQKIVLAREI 423

Query: 419 DRNPDLLIVSQPTRGLDVGAIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHD 478
           + NPD+L++ QPTRG+D+GAIEYIH R++  R +GKAVL++S ELDEI ++SDRI V+ D
Sbjct: 424 ECNPDVLLIGQPTRGVDIGAIEYIHNRIMDMRAQGKAVLLVSVELDEIRSLSDRIIVMFD 483

Query: 479 GQIQGIVSPETTTKQELGILMVGGN 503
           G + G   PE  T+Q+LG+LM G N
Sbjct: 484 GNVVGERGPE-ATEQDLGLLMAGVN 507



 Score = 90.9 bits (224), Expect = 1e-22
 Identities = 72/249 (28%), Positives = 129/249 (51%), Gaps = 17/249 (6%)

Query: 261 IKDLNIKESRGSLKV-KGLSLDVRAGEIVGVAGIDGNGQTELVKAITGLTKVDSGSIKLH 319
           I+ + + +S G +   K + L V  G I G+ G +G G++ L+  + G    DSG+IK+ 
Sbjct: 9   IELIGVNKSFGPVHANKDIDLVVGKGSIHGIIGENGAGKSTLMSILYGFYHADSGTIKID 68

Query: 320 NKDITNQRPRKITEQSVGHVPEDRHRDGLVLE-MTVAENIALQTYYKPPMSKYGFLDYNK 378
            K  T    +    Q +G V    H+  ++++  TV EN+ L        ++ G L  + 
Sbjct: 69  GKATTIPDSKSAISQGIGMV----HQHFMLVDPFTVLENVVLG-------AEGGALLKDG 117

Query: 379 INSHARELM---EEFDVRGAGEWVSASSLSGGNQQKAIIAREIDRNPDLLIVSQPTRGLD 435
           + +  REL    +E+D+    + V    L  G QQ+  I + + R  D+LI+ +PT  L 
Sbjct: 118 VANARRELKRLADEYDMTIDPDAV-VGELPVGLQQRVEILKALYRGADILILDEPTGVLT 176

Query: 436 VGAIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHDGQIQGIVSPETTTKQEL 495
               +++ + L   RD+GK VL+I+ +L EI++V+D ++V+  G++        T+ +EL
Sbjct: 177 PSEADHLFRILRVLRDQGKTVLLITHKLREIMDVTDTVSVMRRGEMVASRKTAQTSMEEL 236

Query: 496 GILMVGGNI 504
             LMVG ++
Sbjct: 237 AELMVGRSV 245


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: 750
Number of extensions: 43
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 506
Length of database: 514
Length adjustment: 34
Effective length of query: 472
Effective length of database: 480
Effective search space:   226560
Effective search space used:   226560
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 Sep 24 2021. The underlying query database was built on Sep 17 2021.

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Steps (tab-delimited)
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Protein sequences (fasta format)
Organisms (tab-delimited)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources