GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Methanothermobacter thermautotrophicus str. Delta H

Align (R)-citramalate synthase (EC 2.3.3.21) (characterized)
to candidate WP_010877238.1 MTH_RS07810 homocitrate synthase family protein

Query= BRENDA::Q58787
         (491 letters)



>NCBI__GCF_000008645.1:WP_010877238.1
          Length = 391

 Score =  375 bits (963), Expect = e-108
 Identities = 183/368 (49%), Positives = 259/368 (70%)

Query: 3   VRIFDTTLRDGEQTPGVSLTPNDKLEIAKKLDELGVDVIEAGSAITSKGEREGIKLITKE 62
           + I+DTTLRDGEQTPGV L   +KLEIA+KLDELG+  IE+G  + S+ ER  +K I  E
Sbjct: 20  ITIYDTTLRDGEQTPGVCLGTEEKLEIARKLDELGIHQIESGFPVVSEQERVSVKSIANE 79

Query: 63  GLNAEICSFVRALPVDIDAALECDVDSVHLVVPTSPIHMKYKLRKTEDEVLETALKAVEY 122
           GLNAEI +  R    DIDAA++CDVD V   + TS +H+K+KL+ T +E L   + ++EY
Sbjct: 80  GLNAEILALCRTKKDDIDAAIDCDVDGVITFMATSDLHLKHKLKLTREEALNVCMNSIEY 139

Query: 123 AKEHGLIVELSAEDATRSDVNFLIKLFNEGEKVGADRVCVCDTVGVLTPQKSQELFKKIT 182
           AK+HGL +  SAEDATR+D++FL +++ + E  GADRV + DTVG ++PQ    L +++ 
Sbjct: 140 AKDHGLFLAFSAEDATRTDLDFLKQIYRKAENYGADRVHIADTVGAISPQGMDYLVRELR 199

Query: 183 ENVNLPVSVHCHNDFGMATANTCSAVLGGAVQCHVTVNGIGERAGNASLEEVVAALKILY 242
            ++ + +++HCHNDFGMA +N+ + +L G      TVNGIGERAGN SLEE++ AL+I+Y
Sbjct: 200 RDIKVDIALHCHNDFGMALSNSIAGLLAGGTAVSTTVNGIGERAGNTSLEELIMALRIIY 259

Query: 243 GYDTKIKMEKLYEVSRIVSRLMKLPVPPNKAIVGDNAFAHEAGIHVDGLIKNTETYEPIK 302
             D    +  LYE+SR+V +  ++ VP NK IVG N F HE+GIHVD +I+   TYEP  
Sbjct: 260 EVDLGFNIGVLYELSRLVEKHTRMKVPENKPIVGRNVFRHESGIHVDAVIEEPLTYEPFL 319

Query: 303 PEMVGNRRRIILGKHSGRKALKYKLDLMGINVSDEQLNKIYERVKEFGDLGKYISDADLL 362
           PEM+G++R+I+LGKHSG +A+K KL+  GI+V+ ++L +I E VK+  + GKYI+D    
Sbjct: 320 PEMIGHQRKIVLGKHSGCRAVKAKLEEYGIDVTRDELCRIVEEVKKNREKGKYINDELFY 379

Query: 363 AIVREVTG 370
            IV+ V G
Sbjct: 380 RIVKSVRG 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: 546
Number of extensions: 25
Number of successful extensions: 1
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 Jul 25 2024. The underlying query database was built on Jul 25 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