GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cyclodeaminase in Desulfovibrio vulgaris Hildenborough

Align LOR/SDH bifunctional enzyme conserved domain-containing protein (characterized, see rationale)
to candidate 208792 DVU3268 conserved hypothetical protein

Query= uniprot:Q6LXX7
         (415 letters)



>MicrobesOnline__882:208792
          Length = 420

 Score =  192 bits (489), Expect = 1e-53
 Identities = 132/377 (35%), Positives = 191/377 (50%), Gaps = 56/377 (14%)

Query: 85  PALKDSVLPDGFYSTTNHPTHVKVND-EWIEVANPKMDAVIVVYPEEKRAETKVIRKVKK 143
           P   D V P G+++T+  P ++ V    W+ +   +MD VI   P+    E    R++K 
Sbjct: 25  PGPADGVAPGGYHATSIFPEYLHVEQGRWVLLERSRMDCVIRQNPDGT-LEVVEFRRLKA 83

Query: 144 GDFVLIGHN-----GIRVMPPEKSREA-------------------GQLFEFM------- 172
           GD V +G       GI V P   S  A                   G+  +         
Sbjct: 84  GDLVALGRGEHAEEGILVHPAGFSASASDEETGPDATPRAPTSPPCGRCGDASVPASAVP 143

Query: 173 -NSEVSSEKPKEAIIKRIAKE---------MHEIREEYKKTGTGGIAIVGGPAIIHTGGG 222
             S  S+++   A    I++E         ++EI    ++ G   I  V GPA++     
Sbjct: 144 PGSPASTQEQPFAFRTGISRETSFSIDYDTLYEILRHDRENGF--IVWVAGPAVVFDADA 201

Query: 223 P-ALAKMVELGYIQAILAGNALATHDIESALYGTSLGVNIKTAKPVTGGHKHHIYAINAI 281
             A A +VE GY+ A+LAGNALATHD+E ALYGT+LG  I   +    GH HH+  INA+
Sbjct: 202 RNAFASLVEQGYVHALLAGNALATHDMEGALYGTALGQGIYHKRQAPMGHYHHLDCINAV 261

Query: 282 NDAGNIKNAVESGVLKEGIMYQCIKNNIPYVLAGSIRDDGPIPDVITDSMVAQDKMRTTV 341
            +AG I  AV SG++++G+M+  +K  +P+VLAGSIRDDGP+PDVI D   AQD MR  V
Sbjct: 262 REAGGIAAAVRSGLIRDGVMHAVVKYGVPFVLAGSIRDDGPLPDVIPDVYDAQDAMRQLV 321

Query: 342 MDKKMVIMLSTLLHSVATGNLMPSY----------IKTVCVDIQPSTVTKLMDRGTSQAI 391
                V+ L+T LH++ATGN+ PSY          +    VD+      KL DRG+  A 
Sbjct: 322 SRATTVVALATQLHTIATGNMTPSYQVLEDGGVRPVHFFVVDMSEFAAGKLADRGSLSAR 381

Query: 392 GVVTDVGVFLVLLLKEL 408
            ++T+V  F+V + + L
Sbjct: 382 AILTNVQDFVVNVTRAL 398


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: 367
Number of extensions: 11
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: 415
Length of database: 420
Length adjustment: 32
Effective length of query: 383
Effective length of database: 388
Effective search space:   148604
Effective search space used:   148604
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 Apr 09 2024. The underlying query database was built on Apr 09 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