GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Rhodopseudomonas palustris CGA009

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_011160139.1 TX73_RS23540 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000195775.1:WP_011160139.1
          Length = 397

 Score =  276 bits (705), Expect = 1e-78
 Identities = 155/344 (45%), Positives = 200/344 (58%), Gaps = 2/344 (0%)

Query: 18  DTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIAREELDA 77
           DTTLRDGEQ PGVA +  EK+ IAR L   GV  IEAG  A    E+ AIR I    L  
Sbjct: 26  DTTLRDGEQAPGVAFSTAEKVAIARALARAGVPEIEAGTPAMGVDEIAAIRAIVEAGLPL 85

Query: 78  EVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREVVEYARDH 137
              +  RM   DVDAA++A    V++ VP S+V +  KL   R   +E  + VV YARD 
Sbjct: 86  TTIAWCRMRTEDVDAALKAGVAMVNVSVPVSDVQIAAKLGGKRSNAIETVKRVVGYARDR 145

Query: 138 GLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVKKLRERVG 197
           GL V +  ED +R + E+L EV      +GA R    DT+ V+ P      +  LR    
Sbjct: 146 GLDVAVGGEDSSRADPEFLAEVIATAKASGARRFRIADTLSVLDPFSSHALLATLR--AS 203

Query: 198 EDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVVLEELYGV 257
            D+ L  H HDD G+ATANT+AA+RAGA    VTV G+GERAGNA LEEV V L++LYG 
Sbjct: 204 TDLELEFHGHDDLGLATANTLAALRAGASHASVTVIGLGERAGNAPLEEVAVALKQLYGR 263

Query: 258 DTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDESTYEPIPPE 317
           DTGI    L  ++ LV       +P NKA+VGE+ FTHESGIH DG+LKD+ TY+ + P 
Sbjct: 264 DTGIVLSELGNVADLVATAAARTIPLNKAIVGEHVFTHESGIHVDGLLKDQRTYQSLDPN 323

Query: 318 KVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKR 361
             G   R V+GKH G S I   L ++ +    ++   IL +++R
Sbjct: 324 LFGRSNRIVIGKHSGLSAITSSLAKLDLPATADEAQGILAKVRR 367


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: 474
Number of extensions: 29
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: 509
Length of database: 397
Length adjustment: 33
Effective length of query: 476
Effective length of database: 364
Effective search space:   173264
Effective search space used:   173264
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