GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysA in Methylocystis bryophila S285

Align Diaminopimelate decarboxylase; DAP decarboxylase; DAPDC; EC 4.1.1.20 (uncharacterized)
to candidate WP_085770944.1 B1812_RS06935 type III PLP-dependent enzyme

Query= curated2:Q9Z661
         (421 letters)



>NCBI__GCF_002117405.1:WP_085770944.1
          Length = 380

 Score =  125 bits (314), Expect = 2e-33
 Identities = 113/372 (30%), Positives = 168/372 (45%), Gaps = 31/372 (8%)

Query: 28  PCYVYSHSYLTERARRFTKALDGAGKGKSLVAFAVKANPSQAILASFAKEGLGADVVSAG 87
           PC V     + +  R F++AL       + V +AVKANP+  +L+  A  G   D  S  
Sbjct: 21  PCLVVDLDVVRDNYRDFSRALPD-----TRVYYAVKANPAPEVLSLLASLGSSFDTASVA 75

Query: 88  EIRRAVHAGIPPERIVFSGVGKTAEEMRYALEIGIGQFNIESVSEIEMLAEVATSLGKKA 147
           EI  A+ AG  PERI F    K   ++  A ++G+  F ++S +E+E +A VA     ++
Sbjct: 76  EIELALAAGASPERISFGNTIKKERDVARAYQLGVRLFAVDSEAEVEKIARVA----PRS 131

Query: 148 AVALRINPDVDPHTHAKIATGKADTKFGIAAEDALSAYEKLASYPSLKIQGIASHIGSQI 207
            V  RI  D         A      KFG A E A    E LA    L   G++ H+GSQ 
Sbjct: 132 KVFCRILCD------GSGAEWPLSRKFGCAPEMAPRVLE-LAQANGLIAYGLSFHVGSQQ 184

Query: 208 TDLAPFEAAAERIYEIITALEKAGHAIETADLGGGLGVRYKDDQPEPPSVEAYGEMIKR- 266
            +   ++ A E    I   L + G  ++  +LGGG   RY    P+   V  YG  I R 
Sbjct: 185 PNPRMWDKALESCANIFRELAERGVYLQMVNLGGGFPTRYLKSVPK---VRIYGNAIFRA 241

Query: 267 VTKGWNCRL---IFEPGRSLIANAGVLLSKVIRI---KESKTARFVILD-AAMNDLVRPT 319
           ++K +  RL   I EPGR ++ NAG++ ++V+ I    +    R+V LD    N L   T
Sbjct: 242 LSKHFGNRLPETIIEPGRGMVGNAGIIEAEVVLISKKSDDDPLRWVFLDIGKFNGLAETT 301

Query: 320 LYDAYHEIKAVTPSAQTYQADIVGPVCETGDIFARNRSIS---AVKADDLMAIMSAGAYG 376
                + I+     A      I GP C++ DI           +++    + I   GAY 
Sbjct: 302 DEMIRYPIRTPVDGAAVGPCVIAGPSCDSVDILYEKTPYELPVSLEIGAKVLIEGTGAYT 361

Query: 377 ATMAS-AYNSRP 387
            T +S A+N  P
Sbjct: 362 TTYSSIAFNGFP 373


Lambda     K      H
   0.317    0.132    0.372 

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: 342
Number of extensions: 15
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: 421
Length of database: 380
Length adjustment: 31
Effective length of query: 390
Effective length of database: 349
Effective search space:   136110
Effective search space used:   136110
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 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