GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Echinicola vietnamensis KMM 6221, DSM 17526

Align (R)-citramalate synthase (EC 2.3.3.21) (characterized)
to candidate Echvi_3833 Echvi_3833 Isopropylmalate/homocitrate/citramalate synthases

Query= BRENDA::Q58787
         (491 letters)



>FitnessBrowser__Cola:Echvi_3833
          Length = 390

 Score =  288 bits (737), Expect = 2e-82
 Identities = 172/376 (45%), Positives = 226/376 (60%), Gaps = 13/376 (3%)

Query: 3   VRIFDTTLRDGEQTPGVSLTPNDKLEIAKKLDELGVDVIEAGSAITSKGEREGIKLITKE 62
           V IFDTTLRDGEQ PG  L    K+EIA++L+ LGVDVIEAG  I+S G+ + +  I+K 
Sbjct: 6   VLIFDTTLRDGEQVPGCKLNTPQKIEIARQLESLGVDVIEAGFPISSPGDFKSVVEISKS 65

Query: 63  GLNAEICSFVRALPVDIDAALE----CDVDSVHLVVPTSPIHMKYKLRKTEDEVLETALK 118
                IC   R +  DI+ A E         +H  + TSP H+KYK + T D++LE A+ 
Sbjct: 66  VSEPIICGLSRGVAKDIEVAAEALKYAKRPRIHTGIGTSPSHIKYKFKSTPDQILERAVA 125

Query: 119 AVEYAKEHGLIVELSAEDATRSDVNFLIKLFNEGEKVGADRVCVCDTVGVLTPQKSQELF 178
           AV++AK     VE  AEDA R+D  +L ++     K GA  + + DT G   P +     
Sbjct: 126 AVKHAKSFVEDVEFYAEDAGRTDNEYLARICEAVVKAGATVLNIPDTTGYCLPDEYGAKI 185

Query: 179 KKITENV----NLPVSVHCHNDFGMATANTCSAVLGGAVQCHVTVNGIGERAGNASLEEV 234
           K + +NV    N+ +S HCHND G+ATAN+ SAV+ GA Q   T+NGIGERAGN SLEEV
Sbjct: 186 KYLMDNVKGIENVIISAHCHNDLGLATANSISAVMNGARQIECTINGIGERAGNTSLEEV 245

Query: 235 VAALK---ILYGYDTKIKMEKLYEVSRIVSRLMKLPVPPNKAIVGDNAFAHEAGIHVDGL 291
              +K    L  Y+ KI    L  +SR+VS  M + V PNKAIVG NAFAH +GIH DG+
Sbjct: 246 AMIMKQHPRLNVYN-KINSRLLNPISRLVSERMGMHVQPNKAIVGSNAFAHSSGIHQDGV 304

Query: 292 IKNTETYEPIKPEMVG-NRRRIILGKHSGRKALKYKLDLMGINVSDEQLNKIYERVKEFG 350
           IKN ETYE I PE VG     I+L   SGR AL ++L  +G  ++  QL+ IY+   E  
Sbjct: 305 IKNRETYEIIDPEEVGVTESMIVLTARSGRAALAFRLHKIGYTITKLQLDDIYQLFLEHA 364

Query: 351 DLGKYISDADLLAIVR 366
           D+ K I+D DL  I++
Sbjct: 365 DMKKEITDEDLHEIMK 380


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: 459
Number of extensions: 25
Number of successful extensions: 5
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: 390
Length adjustment: 32
Effective length of query: 459
Effective length of database: 358
Effective search space:   164322
Effective search space used:   164322
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 09 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