GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Acidovorax sp. GW101-3H11

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate Ac3H11_4785 Glycerol-3-phosphate ABC transporter, ATP-binding protein UgpC (TC 3.A.1.1.3)

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4785
          Length = 334

 Score =  281 bits (720), Expect = 1e-80
 Identities = 164/363 (45%), Positives = 222/363 (61%), Gaps = 32/363 (8%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA L+L ++TK Y   G      +  ++ ++ DGEF+V+VGPSGCGKST LRM+AGLE +
Sbjct: 1   MASLSLRNITKRY-GHGPKANQVIHGVNAEVKDGEFVVIVGPSGCGKSTLLRMVAGLEEI 59

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           + GELR+ DRV+N +    RDIAMVFQ+YALYPH +   NM++GL+ +  +P DEI+ RV
Sbjct: 60  SGGELRIGDRVVNDLEPAQRDIAMVFQNYALYPHMTNFENMAYGLKIAK-VPKDEIKARV 118

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
           ++   +L +  LL+RKP +LSGGQ+QRVA+GRAIVR P+VFL DEPLSNLDAKLRA+ R 
Sbjct: 119 DKAAKILELGHLLERKPRELSGGQRQRVAMGRAIVRQPQVFLFDEPLSNLDAKLRAQTRL 178

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E+Q+L  ELG+T+++VTHDQ EAMT+  R+ V++ G ++Q GTP + YH P   FVA FI
Sbjct: 179 EIQKLHRELGITSLFVTHDQVEAMTLAQRMIVMNAGNMEQFGTPEEVYHTPATTFVASFI 238

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRT 300
           G P MNL                       ++  G   G  LGIRPE + V  R  G   
Sbjct: 239 GSPPMNLL----------------------KNAPGAQPGTILGIRPEHLDV--RSEG--- 271

Query: 301 FDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFDG 360
           +   V  VE  G E  ++ R ++G++         G    E      V    D +H FD 
Sbjct: 272 WAVTVETVELLGAERLIYGR-INGEQ--VIVRVEEGTHSPEPDSVIHVQPRADRLHAFDA 328

Query: 361 ETG 363
            TG
Sbjct: 329 ATG 331


Lambda     K      H
   0.316    0.136    0.384 

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: 389
Number of extensions: 20
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 383
Length of database: 334
Length adjustment: 29
Effective length of query: 354
Effective length of database: 305
Effective search space:   107970
Effective search space used:   107970
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: 49 (23.5 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