GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cyclodeaminase in Desulfacinum hydrothermale DSM 13146

Align LOR/SDH bifunctional enzyme conserved domain-containing protein (characterized, see rationale)
to candidate WP_084057564.1 B9A12_RS09070 hypothetical protein

Query= uniprot:Q6LXX7
         (415 letters)



>NCBI__GCF_900176285.1:WP_084057564.1
          Length = 371

 Score =  187 bits (476), Expect = 3e-52
 Identities = 123/351 (35%), Positives = 188/351 (53%), Gaps = 35/351 (9%)

Query: 88  KDSVLPDGFYSTTNHPTHVKVND-EWIEVANPKMDAVIVVYPEEKRAETKVIRKVKKGDF 146
           K  V P+G+++T+  P +  V    W  +   +MD V+V  P+  R +    R+++ GD 
Sbjct: 30  KAGVAPEGYHATSVFPEYFHVAPGRWEILRESRMDCVVVQRPDG-RLDVVEFRRLQPGDR 88

Query: 147 VLIGHNGIRVMPPEKSREAGQLFEFMNSE----VSSEKPKEAIIKRIAKEMH---EIREE 199
           V +G            RE  +   F+++E    +S    K A   R+ +E     +  E 
Sbjct: 89  VAVGR-----------RENAEEGIFVHAEAFQGMSGTGDKFAFRTRLTRETSFSIDYDEF 137

Query: 200 YK----KTGTGGIAIVGGPAIIHTGGG-PALAKMVELGYIQAILAGNALATHDIESALYG 254
           Y     +   G I  V GPA++       A + ++  GY+ A+LAGNALATHD+E AL+G
Sbjct: 138 YDLLVHERNHGTIVWVLGPAVVFDQDARSAFSSLIRRGYVHALLAGNALATHDLEGALFG 197

Query: 255 TSLGVNIKTAKPVTGGHKHHIYAINAINDAGNIKNAVESGVLKEGIMYQCIKNNIPYVLA 314
           T+LG  I + +    GH HH+ AIN + + G+I+ A++ GV+ +G+M+  +   IP VLA
Sbjct: 198 TALGQEIYSKRSAPLGHYHHLDAINRLRELGSIEEAMQRGVVTDGVMHAAVTQGIPVVLA 257

Query: 315 GSIRDDGPIPDVITDSMVAQDKMRTTVMDKKMVIMLSTLLHSVATGNLMPSY-------- 366
           GSIRDDGP+P VI D   AQD+MR  V     V+ L+T LH++ATGN+ PSY        
Sbjct: 258 GSIRDDGPLPGVIADVYEAQDRMRDQVRRATTVVALATQLHAIATGNMAPSYRVLDDGTV 317

Query: 367 --IKTVCVDIQPSTVTKLMDRGTSQAIGVVTDVGVFLVLLLKELERLELQE 415
             +    VD+    V KL +RG+  A  ++T+V  F+V + + L R E  E
Sbjct: 318 RPVYFYSVDMSEFAVQKLANRGSLTARSILTNVQDFMVTVERGLRRRETNE 368


Lambda     K      H
   0.317    0.136    0.380 

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: 287
Number of extensions: 14
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: 415
Length of database: 371
Length adjustment: 31
Effective length of query: 384
Effective length of database: 340
Effective search space:   130560
Effective search space used:   130560
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

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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