GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Malonomonas rubra DSM 5091

Align (R)-citramalate synthase (EC 2.3.3.21) (characterized)
to candidate WP_072910006.1 BUB13_RS17220 homocitrate synthase

Query= BRENDA::Q58787
         (491 letters)



>NCBI__GCF_900142125.1:WP_072910006.1
          Length = 375

 Score =  271 bits (692), Expect = 4e-77
 Identities = 144/343 (41%), Positives = 211/343 (61%)

Query: 5   IFDTTLRDGEQTPGVSLTPNDKLEIAKKLDELGVDVIEAGSAITSKGEREGIKLITKEGL 64
           I DTTLRDGEQT GV+ +  +K  IA+ LDE+GV  +E G     + E+  I+ +   GL
Sbjct: 11  IDDTTLRDGEQTAGVAFSLEEKKRIARMLDEIGVGELECGIPAMGEQEQASIRALVDMGL 70

Query: 65  NAEICSFVRALPVDIDAALECDVDSVHLVVPTSPIHMKYKLRKTEDEVLETALKAVEYAK 124
           NA + ++ RA+  DI+A+L+  V++V + +  S  HMK+KL K+   V E    A+ +AK
Sbjct: 71  NARLMTWNRAVISDIEASLKTGVEAVDISLSVSDQHMKHKLGKSRQWVKEQLKVALGFAK 130

Query: 125 EHGLIVELSAEDATRSDVNFLIKLFNEGEKVGADRVCVCDTVGVLTPQKSQELFKKITEN 184
           +H L V +  ED++R+D++FL++L    E  GADR   CDT+G+L P  +  + K + + 
Sbjct: 131 KHNLYVSVGGEDSSRADLDFLVELLQIAENEGADRFRFCDTLGILDPFATYGMVKYLYDR 190

Query: 185 VNLPVSVHCHNDFGMATANTCSAVLGGAVQCHVTVNGIGERAGNASLEEVVAALKILYGY 244
             L + VH HND GMATAN  + +  GA   + TVNG+GERAGNA+LEEVV ALK   G 
Sbjct: 191 TGLDLEVHTHNDLGMATANAIAGIRAGARFVNTTVNGLGERAGNAALEEVVMALKHACGR 250

Query: 245 DTKIKMEKLYEVSRIVSRLMKLPVPPNKAIVGDNAFAHEAGIHVDGLIKNTETYEPIKPE 304
           D  I   +  E+SR VS+    PVP  KA+VG+  F+HE+G+H DG+IK+   YE   P 
Sbjct: 251 DPHIDTSRFVEISRYVSQASHHPVPDWKAVVGEKVFSHESGLHADGVIKDARNYEGFDPA 310

Query: 305 MVGNRRRIILGKHSGRKALKYKLDLMGINVSDEQLNKIYERVK 347
            VG +R ++LGKHSG   L  +L  + I+     ++ +  +V+
Sbjct: 311 EVGLQRYMVLGKHSGSHGLLQRLKQLDIDPQQLDVDALLSQVR 353


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: 454
Number of extensions: 15
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: 375
Length adjustment: 32
Effective length of query: 459
Effective length of database: 343
Effective search space:   157437
Effective search space used:   157437
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