GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Methyloferula stellata AR4T

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_020177082.1 A3OQ_RS0119280 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000385335.1:WP_020177082.1
          Length = 399

 Score =  287 bits (735), Expect = 4e-82
 Identities = 160/376 (42%), Positives = 213/376 (56%), Gaps = 4/376 (1%)

Query: 1   MREANADADPPDEVRIF--DTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAA 58
           M   NA A       +F  DTTLRDGEQ PGVA T +EK+ IA  L   GV  IEAG  A
Sbjct: 1   MSSGNASARSGLRTPVFLNDTTLRDGEQAPGVAFTIDEKVAIAEALATAGVPEIEAGTPA 60

Query: 59  ASEGELKAIRRIAREELDAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRM 118
               E+ AI  I  + L     +  RM++ D+DAAV      V+  VP S++ +K K   
Sbjct: 61  MGAEEIAAINAIVGQNLPLTPIAWCRMLRADIDAAVATGVRMVNASVPVSDIQLKAKFGA 120

Query: 119 DREEVLERAREVVEYARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVG 178
            R   L     VV YARD GL V +  ED +R +  +L EV DA   AGA R  + DT+G
Sbjct: 121 GRAHALALIENVVPYARDCGLEVAVGGEDASRADPGFLAEVLDAVARAGARRFRFADTLG 180

Query: 179 VMAPEGMFLAVKKLRERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGER 238
           V+ P   +  V+ LR     D+ + +H HDD G+ATANT+AA+RAGA    VTV G+GER
Sbjct: 181 VLDPFATYAMVEHLRRH--SDLEIEIHAHDDLGLATANTLAALRAGASHASVTVVGLGER 238

Query: 239 AGNAALEEVVVVLEELYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESG 298
           AGNA LEEV V +  LYG++TGI    L+ +++ V +  G  +P  KA+VG+  FTHESG
Sbjct: 239 AGNAPLEEVAVAVSALYGLETGIDLRSLSAVAQTVMKAAGRAIPEAKAIVGDAVFTHESG 298

Query: 299 IHADGILKDESTYEPIPPEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRR 358
           IH DG+LKD   YE + P  +G   R VLGKH G   +    K++G+DV  ++   IL  
Sbjct: 299 IHVDGLLKDRKCYEALDPAVLGRTHRLVLGKHSGLGAVVNAFKELGIDVQSDEAKAILAL 358

Query: 359 LKRLGDRGKRITEADL 374
           ++   +R K    A +
Sbjct: 359 VRAYAERTKAAVPASM 374


Lambda     K      H
   0.315    0.134    0.367 

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: 480
Number of extensions: 28
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: 509
Length of database: 399
Length adjustment: 33
Effective length of query: 476
Effective length of database: 366
Effective search space:   174216
Effective search space used:   174216
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: 51 (24.3 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