GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysA in Methylobacterium sp. 4-46

Align Diaminopimelate decarboxylase; DAP decarboxylase; DAPDC; EC 4.1.1.20 (uncharacterized)
to candidate WP_026190940.1 M446_RS02180 type III PLP-dependent enzyme

Query= curated2:Q9JXM2
         (414 letters)



>NCBI__GCF_000019365.1:WP_026190940.1
          Length = 388

 Score =  111 bits (278), Expect = 3e-29
 Identities = 105/348 (30%), Positives = 157/348 (45%), Gaps = 27/348 (7%)

Query: 39  AFAALNP--LVCYAVKANGNLSIIKHFASLGSGFDIVSGGELARVLAAGGDAAKTIFSGV 96
           AFA   P   V YAVKAN    ++   ASLGS FD  S  E+   LAAG  A +  F   
Sbjct: 36  AFARALPDTRVFYAVKANPAPEVLGLLASLGSCFDTASVAEIQMALAAGATADRISFGNT 95

Query: 97  GKSEAEIEFALNAGVKCFNMESIPEIDRIQKVAARLGKTAP----VSLRINPDVDAKTHP 152
            K E  I  AL  GV+ F ++   E+++I + AA     AP    V  RI  D      P
Sbjct: 96  IKKERCIARALALGVRLFAVDCEAEVEKIARAAA-CADVAPEEVQVFCRILCDGAGAEWP 154

Query: 153 YISTGLKANKFGIAYADALEAYHYAAQQPNLKIIGIDCHIGSQLTDLSPLVEACERILIL 212
                  + KFG     A++   +A +Q  L+  G+  H+GSQ  +      A     ++
Sbjct: 155 L------SRKFGCVPDMAVDVLEHAHRQ-GLRAYGVSFHVGSQQGNTEAWDGALASAAMI 207

Query: 213 VDALAAEGIVLEHLDLGGGVGIVYQDENVPDL----GAYAQAVQKLIGTRRLKLILEPGR 268
               A  GI L  ++LGGG    Y  E VP +    GA  +A+ K  G R  + I+EPGR
Sbjct: 208 FRECAERGIALAMVNLGGGFPTKYLKE-VPGVESYGGAIFRALTKHFGNRMPETIIEPGR 266

Query: 269 SLVGNAGSLLTRVEFV----KYGEEKNFVMVDAAMNDLMRPALYDAYHHIEAVETKDIAT 324
            +VGNAG +   V  V    +  +E  +V +D      +   + ++  +    +  +   
Sbjct: 267 GMVGNAGIIEAEVILVSKKSEAADEVRWVYLDIGKFGGLAETMDESIRYRIRTDHDEDRM 326

Query: 325 LTANIVGPICETGDFLGK----DRTIACEEGDLLLIRSAGAYGASMAS 368
           +   + GP C++ D L +       ++   GD +LI  AGAY  + A+
Sbjct: 327 VPCVLAGPTCDSADVLYEKIPYPLPVSLSIGDKVLIEGAGAYTTTYAA 374


Lambda     K      H
   0.319    0.136    0.388 

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: 390
Number of extensions: 23
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: 414
Length of database: 388
Length adjustment: 31
Effective length of query: 383
Effective length of database: 357
Effective search space:   136731
Effective search space used:   136731
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 Apr 10 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