GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Methanobacterium lacus AL-21

Align (R)-citramalate synthase (EC 2.3.3.21) (characterized)
to candidate WP_013645641.1 METBO_RS10235 2-isopropylmalate synthase

Query= BRENDA::Q58787
         (491 letters)



>NCBI__GCF_000191585.1:WP_013645641.1
          Length = 391

 Score =  360 bits (924), Expect = e-104
 Identities = 175/368 (47%), Positives = 252/368 (68%)

Query: 3   VRIFDTTLRDGEQTPGVSLTPNDKLEIAKKLDELGVDVIEAGSAITSKGEREGIKLITKE 62
           + ++DTTLRDGEQTPGV L   +KL+IAKKLDE+G+  IEAG  + SK E++ +  I  E
Sbjct: 20  ITVYDTTLRDGEQTPGVCLRTPEKLKIAKKLDEVGIHQIEAGFPVVSKEEKKSVTAIVNE 79

Query: 63  GLNAEICSFVRALPVDIDAALECDVDSVHLVVPTSPIHMKYKLRKTEDEVLETALKAVEY 122
            LNA+I    R    DID A++CDVD +   + TS +H+K+K++ + +E+L   + ++E+
Sbjct: 80  DLNAQILCLSRTKKSDIDTAIDCDVDGIITFMSTSDLHLKHKIKMSREEILNVCMNSIEH 139

Query: 123 AKEHGLIVELSAEDATRSDVNFLIKLFNEGEKVGADRVCVCDTVGVLTPQKSQELFKKIT 182
           AK+HGL V  SAEDATR+D++FL K++ + +  G DRV + DTVG ++P     L K++ 
Sbjct: 140 AKDHGLFVAFSAEDATRTDLDFLKKMYKKADDYGVDRVHIADTVGAISPYGMDYLVKQLR 199

Query: 183 ENVNLPVSVHCHNDFGMATANTCSAVLGGAVQCHVTVNGIGERAGNASLEEVVAALKILY 242
             +N  +++HCHNDFGMA AN+ + +L GA     TVNGIGERAGNA+LEE+V  LK +Y
Sbjct: 200 STINAEIALHCHNDFGMALANSIAGLLAGANAVSTTVNGIGERAGNAALEELVMTLKFIY 259

Query: 243 GYDTKIKMEKLYEVSRIVSRLMKLPVPPNKAIVGDNAFAHEAGIHVDGLIKNTETYEPIK 302
           G D    + K  E+S++V  L  + +P NK IVG N F HE+GIHVD +I+   TYEP  
Sbjct: 260 GVDLGFDVSKFCELSKLVESLTHMDIPYNKPIVGKNIFRHESGIHVDAVIEEPLTYEPFL 319

Query: 303 PEMVGNRRRIILGKHSGRKALKYKLDLMGINVSDEQLNKIYERVKEFGDLGKYISDADLL 362
           PE++G+RR+I+LGKHSG +A++ KL+  GI+V+ ++L KI E+VK   + G YI+D    
Sbjct: 320 PELIGHRRQIVLGKHSGCRAVRAKLNECGIDVTKDELCKIVEQVKSKREEGNYINDELFN 379

Query: 363 AIVREVTG 370
           +IV  V G
Sbjct: 380 SIVASVRG 387


Lambda     K      H
   0.316    0.136    0.373 

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: 547
Number of extensions: 23
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: 491
Length of database: 391
Length adjustment: 32
Effective length of query: 459
Effective length of database: 359
Effective search space:   164781
Effective search space used:   164781
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.

Links

Downloads

Related tools

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