Alignments for a candidate for frcA in Paraburkholderia bryophila 376MFSha3.1

GapMind for catabolism of small carbon sources

Alignments for a candidate for frcA in Paraburkholderia bryophila 376MFSha3.1

Align ABC-type sugar transport system, ATP-binding protein; EC 3.6.3.17 (characterized, see rationale)
to candidate H281DRAFT_00426 H281DRAFT_00426 monosaccharide ABC transporter ATP-binding protein, CUT2 family

Query= uniprot:A0A0C4Y5F6
         (540 letters)



>FitnessBrowser__Burk376:H281DRAFT_00426
          Length = 503

 Score =  409 bits (1052), Expect = e-118
 Identities = 242/506 (47%), Positives = 330/506 (65%), Gaps = 16/506 (3%)

Query: 12  PLLALRNICKTFPGVRALRKVELTAYAGEVHALMGENGAGKSTLMKILSGAYTADPGGEC 71
           PL++++ + K+FPGVRAL  V+     GEVHALMGENGAGKSTLMKIL+G YT D  GE 
Sbjct: 3   PLISVKKLSKSFPGVRALHDVQFDLVEGEVHALMGENGAGKSTLMKILAGVYTRD-SGEI 61

Query: 72  HIDGQRVQIDGPQSARDLGVAVIYQELSLAPNLSVAENIYLGRALQRR-GLVARGDMVRA 130
            + GQ V++  P+ A+  G+ +I+QEL L  +L+VA+NI++GR  + R GL    D + A
Sbjct: 62  LLGGQPVELQSPRDAQAAGIGIIHQELQLMNHLTVAQNIFIGREPRGRLGLFLDEDKLNA 121

Query: 131 CA-PTLARLGADFSPAANVASLSIAQRQLVEIARAVHFEARILVMDEPTTPLSTHETDRL 189
            A   L+R+  +  P A V +L++A +Q+VEIA+A+ F++R+L+MDEPT+ L+  E   L
Sbjct: 122 KAREILSRMHVNIDPRAMVGNLTVASQQMVEIAKALSFDSRVLIMDEPTSALNDAEIAEL 181

Query: 190 FALIRQLRGEGMAILYISHRMAEIDELADRVTVLRDGCFVGTLDRAHLSQAALVKMMVGR 249
           F +IR+L+  G+ ++YISH+M E+ ++ADRVTVLRDG +V T+  A  S  A++ MMVGR
Sbjct: 182 FRIIRELKQRGVGVVYISHKMDELKQIADRVTVLRDGEYVATVAAADTSVEAIIGMMVGR 241

Query: 250 DLSGFYTKTHGQAVEREVMLSVRDVADGRRVKGCSFDLRAGEVLGLAGLVGAGRTELARL 309
            LS         A + E+ L VR++  G  V+  SF LR GE+LG AGL+GAGRTE+AR 
Sbjct: 242 TLSD-VAPAGRAASQGEIALEVRNLHAGPLVRDVSFTLRKGEILGFAGLMGAGRTEVARA 300

Query: 310 VFGADARTRGEVRIANPAGSGGLVTLPAGGPRQAIDAGIAYLTEDRKLQGLFLDQSVHEN 369
           VFGAD    GE+ +     S          P  A+  GI YL+EDRK  GL     V  N
Sbjct: 301 VFGADPVESGEIFVKGAKAS-------IRTPSDAVAHGIGYLSEDRKRFGLATGMDVESN 353

Query: 370 INLIVAARDALGLG-RLNRTAARRRTTEAIDTLGIRVAHAQVNVGALSGGNQQKVMLSRL 428
           I ++   R+ L L   L R   RRR +  I+ L IR   A   V  LSGGNQQK+++++ 
Sbjct: 354 I-VMSNLRNFLSLNFFLRRARMRRRASHFINLLAIRTPSAAQQVRLLSGGNQQKIVIAKW 412

Query: 429 LEIQPRVLILDEPTRGVDIGAKSEIYRLINALAQSGVAILMISSELPEVVGLCDRVLVMR 488
           LE    VL  DEPTRG+D+GAKSEIY+L+ +LA  G AI+MISSELPE++ + DRV+VM 
Sbjct: 413 LERDCDVLFFDEPTRGIDVGAKSEIYKLLRSLADEGKAIVMISSELPEILRMSDRVVVMC 472

Query: 489 EGTLAGEVRPAGSAAETQERIIALAT 514
           EG + GE+ PA  A  TQERI+ LAT
Sbjct: 473 EGRITGEL-PAEQA--TQERIMHLAT 495



 Score = 77.0 bits (188), Expect = 2e-18
 Identities = 62/228 (27%), Positives = 101/228 (44%), Gaps = 8/228 (3%)

Query: 29  LRKVELTAYAGEVHALMGENGAGKSTLMKILSGAYTADPGGECHIDGQRVQIDGPQSARD 88
           +R V  T   GE+    G  GAG++ + + + GA   +  GE  + G +  I  P  A  
Sbjct: 271 VRDVSFTLRKGEILGFAGLMGAGRTEVARAVFGADPVE-SGEIFVKGAKASIRTPSDAVA 329

Query: 89  LGVAVIYQE---LSLAPNLSVAENIYLG--RALQRRGLVARGDMVRACAPTLARLGADFS 143
            G+  + ++     LA  + V  NI +   R         R   +R  A     L A  +
Sbjct: 330 HGIGYLSEDRKRFGLATGMDVESNIVMSNLRNFLSLNFFLRRARMRRRASHFINLLAIRT 389

Query: 144 PAA--NVASLSIAQRQLVEIARAVHFEARILVMDEPTTPLSTHETDRLFALIRQLRGEGM 201
           P+A   V  LS   +Q + IA+ +  +  +L  DEPT  +       ++ L+R L  EG 
Sbjct: 390 PSAAQQVRLLSGGNQQKIVIAKWLERDCDVLFFDEPTRGIDVGAKSEIYKLLRSLADEGK 449

Query: 202 AILYISHRMAEIDELADRVTVLRDGCFVGTLDRAHLSQAALVKMMVGR 249
           AI+ IS  + EI  ++DRV V+ +G   G L     +Q  ++ +   R
Sbjct: 450 AIVMISSELPEILRMSDRVVVMCEGRITGELPAEQATQERIMHLATQR 497


Lambda     K      H
   0.320    0.136    0.382 

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: 588
Number of extensions: 32
Number of successful extensions: 10
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: 540
Length of database: 503
Length adjustment: 35
Effective length of query: 505
Effective length of database: 468
Effective search space:   236340
Effective search space used:   236340
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:

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 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