GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc02869 in Pseudovibrio axinellae Ad2

Align N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized)
to candidate WP_068006976.1 PsAD2_RS14030 ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc02869
         (352 letters)



>NCBI__GCF_001623255.1:WP_068006976.1
          Length = 361

 Score =  291 bits (745), Expect = 2e-83
 Identities = 157/317 (49%), Positives = 209/317 (65%), Gaps = 31/317 (9%)

Query: 17  VGSLQLKTIRKAFGSHEVLKGIDLDVKDGEFVIFVGPSGCGKSTLLRTIAGLEDATSGSV 76
           + S+++K +   FG  EVLK ++L +  GEF++ +G SGCGKSTLL  +AGL D + G +
Sbjct: 1   MNSIEIKDLSLRFGEVEVLKNLNLSIHKGEFLVLLGSSGCGKSTLLNCVAGLLDLSHGQI 60

Query: 77  QIDGVEVGHVAPAKRGIAMVFQSYALYPHLTVKDNMGLGLKQAGVPKAEIEEKVAKAAGM 136
            ID   V    P  RGI MVFQSYALYP ++V+ N+  GLK AG+PKAEI +++ +AA +
Sbjct: 61  FIDERNVTWEEPKDRGIGMVFQSYALYPQMSVRGNLSFGLKNAGIPKAEIAKRIQRAAEI 120

Query: 137 LSLEPYLARRPAELSGGQRQRVAIGRAIVREPKLFLFDEPLSNLDAALRVNTRLEIARLH 196
           L ++  L R+PA LSGGQRQRVAIGRA+VR+  +FLFDEPLSNLDA LR + R+EI RLH
Sbjct: 121 LQIQDLLHRKPAALSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRADLRVEINRLH 180

Query: 197 RSLKATMIYVTHDQVEAMTLADKIVVLNAGRIEQVGSPMELYNRPANLFVAGFIGSPQMN 256
             LK TMIYVTHDQ+EAMTLAD+I V+  G I Q+  P ++YNRP N ++AGFIGSP MN
Sbjct: 181 HRLKNTMIYVTHDQIEAMTLADRIAVMRDGNILQLDVPSQIYNRPINKYIAGFIGSPSMN 240

Query: 257 FIEAAKLGDGE--------------------------AKTIGIRPEHI---GLSRESGDW 287
           F+E  KL  G+                          A T+G+RPEHI     ++E    
Sbjct: 241 FLE-GKLSAGDNPSFIFGDERFDMSRYRFDGEGQQNGATTLGVRPEHIRTGNAAQEMPIS 299

Query: 288 KGKVIH-VEHLGADTII 303
           +  V+  VE +G+DT++
Sbjct: 300 RNIVVEVVEPMGSDTLV 316


Lambda     K      H
   0.320    0.137    0.393 

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: 347
Number of extensions: 12
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: 352
Length of database: 361
Length adjustment: 29
Effective length of query: 323
Effective length of database: 332
Effective search space:   107236
Effective search space used:   107236
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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