GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Hyphomicrobium sulfonivorans WDL6

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate WP_083509566.1 APY04_RS07015 ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_791
         (363 letters)



>NCBI__GCF_001541235.1:WP_083509566.1
          Length = 392

 Score =  161 bits (407), Expect = 3e-44
 Identities = 116/360 (32%), Positives = 172/360 (47%), Gaps = 32/360 (8%)

Query: 3   LALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVTVD 62
           L  + + +  G    L  +SL +  G V  LLG +  GKT+L+RI AG++ PT GRV ++
Sbjct: 46  LTFEDVRRNFGTTQALAGVSLEIDRGEVVCLLGPSGCGKTTLLRIAAGIERPTGGRVLIN 105

Query: 63  GKDVTG----MPVRDRNVAMVYQQFINYPSMKVAANIASPLKLRGEKNIDARVREIASRL 118
           G +V G    +    R+V +++Q F  +P + +A N+A  LK                R+
Sbjct: 106 GHEVAGPSSFVVPEKRSVGLMFQDFALFPHLTIAGNVAFGLKSLPRAEAKREALAALKRV 165

Query: 119 HIDMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFA 178
            ++   D YP  LSGGQQQRVALARAL     +ML+DEP   LD +LR+ ++EE   L  
Sbjct: 166 GLEHMADEYPHVLSGGQQQRVALARALVPRPAVMLMDEPFSGLDVQLRDAMQEETLSLLR 225

Query: 179 AGQSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNL 238
              +T +  T  P EA+ +G    V+  G L+Q G    ++H P  L VAR FS+  +N 
Sbjct: 226 ETGATAMVVTHNPEEAMRIGDRIVVMRAGGLIQQGQAEALYHQPADLFVARLFSE--INE 283

Query: 239 MAASATAQGVRLQGGAELTLPL-----PQGAATAAGLTVGVRASALR-------VHARPG 286
           +A    A G       ++  P+     P G      +T+GVR   +R       +  R  
Sbjct: 284 VAYRVGADG-------KIDTPIGKLSPPAGLQAHDAVTIGVRERDIRLSDNGEGLSGRVL 336

Query: 287 DVSVAGVVELAEISGSDTFVHASTPWGDLVAQLTGVHYFELGTAITLHLDPAQAYVFGAD 346
           D    G V   E+ G + F     P    V +  G   F  G  +   +DP +A VF A+
Sbjct: 337 DAKFLGDVVRLEV-GIEGF---DQPLKVRVRESAG---FRQGHDVRAQIDPERALVFAAE 389


Lambda     K      H
   0.318    0.133    0.375 

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: 286
Number of extensions: 13
Number of successful extensions: 2
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: 363
Length of database: 392
Length adjustment: 30
Effective length of query: 333
Effective length of database: 362
Effective search space:   120546
Effective search space used:   120546
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: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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