GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Pontimonas salivibrio CL-TW6

Align threonine ammonia-lyase (EC 4.3.1.19) (characterized)
to candidate WP_104913117.1 C3B54_RS02615 threonine ammonia-lyase

Query= BRENDA::Q74FW6
         (402 letters)



>NCBI__GCF_002950575.1:WP_104913117.1
          Length = 419

 Score =  335 bits (860), Expect = 1e-96
 Identities = 176/375 (46%), Positives = 251/375 (66%), Gaps = 5/375 (1%)

Query: 26  SHHFSEKLGIPIYFKCENLQRTGAFKIRGALNFMTSQPREALAKGVITASAGNHAQGVAF 85
           S +  E LG+P++ KCENLQRTG++KIRGA N M+    E  A+GV+ ASAGNHAQGVAF
Sbjct: 40  SRYLEELLGVPVFMKCENLQRTGSYKIRGAFNRMSKLSEEERARGVVAASAGNHAQGVAF 99

Query: 86  SADLLGVPSTVFMPESTPPQKVFATRDYGAEVVLTGRNFDEAYAAAVQAQEERGALFVHP 145
           +A  LG+ +T+F P      K+ ATR YGAEVVLTG        AA +  ++ GA+ + P
Sbjct: 100 AAKELGIKATIFTPTGVALPKLQATRAYGAEVVLTGDTMIGPLRAASEFAKQTGAVRIPP 159

Query: 146 FDDPLVMAGQGTIGLEVLQELPDVANILVPIGGGGLIAGIATAIRETHP----HVRIIGV 201
           FD   V+AGQGT+GLE+L ++P+V  ++VPIGGGGL+AG+A+ +++        +++IGV
Sbjct: 160 FDHHDVVAGQGTVGLEILDQMPEVETVVVPIGGGGLMAGVASVMKQRAALEGRSIKVIGV 219

Query: 202 ETAAAPSAHYSLQKGKIVQVPVTVTLADGIAVKKPGVNTFPIIRDLVDEVVLVEEEEIAL 261
           +   A     S++ GKIV+V V  T+ADGIAV KPG   F II+  VDEVV V+++E A 
Sbjct: 220 QATNAAPYPLSIEAGKIVEVSVKPTIADGIAVSKPGELNFDIIKHTVDEVVTVDDDETAR 279

Query: 262 AIVALLERTKLLVEGAGAVPLAALLNRRVTDLSGKTVCVLSGGNIDVKTISVVVERGLVA 321
           AI+ LLER K++VE AGAV +AA+++  V   +G T  +LSGGNID   +  V+ RGL +
Sbjct: 280 AILVLLERAKMVVEPAGAVAVAAVMSGLV-KATGPTAVILSGGNIDPMILERVISRGLAS 338

Query: 322 AGRYLKLKVELDDLPGALARLATEIAEAKANISIITHDRRSKSLPIGKTEVLIELETRGF 381
           +GRY+K+++ L D PG LAR +  +A+  AN+  + H R    L I + E+ + +ETRG 
Sbjct: 339 SGRYMKMRIPLPDRPGQLARTSEIVADENANVVEVLHTRHGTGLQISQVELELHIETRGP 398

Query: 382 EHIQEVISHLQGVGY 396
           EH ++V+  L+  GY
Sbjct: 399 EHAEQVLEALRREGY 413


Lambda     K      H
   0.319    0.137    0.383 

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: 354
Number of extensions: 10
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: 402
Length of database: 419
Length adjustment: 31
Effective length of query: 371
Effective length of database: 388
Effective search space:   143948
Effective search space used:   143948
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: 50 (23.9 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