GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Pyrolobus fumarii 1A

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_014027225.1 PYRFU_RS08315 2-isopropylmalate synthase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000223395.1:WP_014027225.1
          Length = 396

 Score =  372 bits (956), Expect = e-107
 Identities = 192/375 (51%), Positives = 258/375 (68%)

Query: 14  VRIFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIARE 73
           +R+FDTTLRDGEQ  GV L+ ++K+ IA+ LDE+ VD IEAGF A+S+ + K++   ARE
Sbjct: 19  IRVFDTTLRDGEQMAGVELSLDDKIEIAKALDELRVDLIEAGFPASSDIDFKSVLFTARE 78

Query: 74  ELDAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREVVEY 133
              A+V  +AR  K D+D A EAEA  +H+ + TS++H+K KLRM REEVL+RA E VEY
Sbjct: 79  VSHAKVVGLARANKRDIDMAAEAEAHVIHVFIATSDIHMKYKLRMTREEVLQRAVEAVEY 138

Query: 134 ARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVKKLR 193
           A+ +G+ V  S ED TR++ E+L +V+ A +EAGA+ +   DTVGVM P  M   V+ +R
Sbjct: 139 AKSYGVEVLFSAEDATRSDREFLAQVYRAVIEAGAKYINIPDTVGVMLPWEMEDLVRYIR 198

Query: 194 ERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVVLEE 253
            ++  +V + VHCH+DFGMATANT+AAVR GA  V VTVNG GERAGNAALEEVV  L  
Sbjct: 199 SKLPPNVNIDVHCHNDFGMATANTIAAVRGGANGVQVTVNGFGERAGNAALEEVVATLHF 258

Query: 254 LYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDESTYEP 313
             G+ T IR E+L E+S+LV    G+++PPNK +VG+NAF HE+GIH  G+L +  TYEP
Sbjct: 259 KMGLKTNIRLEKLYEVSRLVAAKFGIKLPPNKPIVGDNAFAHEAGIHVHGVLSNPLTYEP 318

Query: 314 IPPEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGKRITEAD 373
           IPPE VG +RR VLG+H G   +   LK +G D   + +  +LRR+K +    KR+TE  
Sbjct: 319 IPPEAVGAKRRIVLGRHSGKHAVEYVLKHLGYDPTPDLVDYVLRRVKEVAPYAKRVTEDL 378

Query: 374 LRAIAEDVLGRPAER 388
           +R I E+ L     R
Sbjct: 379 VRKIVEEFLAERTTR 393


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: 518
Number of extensions: 17
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: 509
Length of database: 396
Length adjustment: 33
Effective length of query: 476
Effective length of database: 363
Effective search space:   172788
Effective search space used:   172788
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