GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CBS in Synechococcus elongatus PCC 7942

Align cysteine synthase (EC 2.5.1.47); cystathionine beta-synthase (EC 4.2.1.22) (characterized)
to candidate Synpcc7942_B2623 Synpcc7942_B2623 cysteine synthase A

Query= BRENDA::F9UT54
         (303 letters)



>FitnessBrowser__SynE:Synpcc7942_B2623
          Length = 329

 Score =  219 bits (559), Expect = 5e-62
 Identities = 124/304 (40%), Positives = 179/304 (58%), Gaps = 5/304 (1%)

Query: 2   LIQHVQELIGHTPLMALPIEVPNH---SHIYAKLEMFNPGGSIKDRLGAYLIEDGLQRGR 58
           ++  + E IG+TPL+ L      +   + +  KLE  NP GS+KDR    LI+    +G 
Sbjct: 4   ILNRLTEWIGNTPLVRLQETAQQYGAIAEVLLKLEYLNPLGSVKDRTALSLIQSARSQGL 63

Query: 59  VNAKTTIIEPTAGNTGIGLALATQAHHLRTILVVPEKFSMEKQVLMQALGAEIVHTPSEE 118
           + A TT+IEPT GNTGIGLA A  A  LR ILV+P++ S E+  L + LGA++V TP+ E
Sbjct: 64  ITAGTTLIEPTTGNTGIGLAFAAAAEQLRLILVMPDRVSAERIRLAKLLGAKVVLTPAAE 123

Query: 119 GIKGAIRKAEALAATISNSYVPMQFKNPANPAAYYHTLAPEILADMPAPITAFVAGAGSG 178
            + G I KA+AL   I +S +  QF+NPANP+ +  T  PEI  D    +   VAG G+G
Sbjct: 124 AMLGCIAKAQALQQQIPDSVILQQFQNPANPSIHQATTGPEIWRDTDGEVDIVVAGVGTG 183

Query: 179 GTFAGVAAYLQAQDSATKAVVVEPEGS-ILNGGPAHAHRTEGIGVEFIPPFFDQVRIDQT 237
           GT  G++ YL+      +++ V+P  S +L+GG A +H+  G+G  F+ P  D+  ID+ 
Sbjct: 184 GTLMGISRYLKPLRPRLQSIAVQPARSPVLSGGAAGSHQLTGMGPNFVSPLVDRSLIDEI 243

Query: 238 LTIADNDAFAQVRHLARDHGLLIGSSSGAALAASLQLATNLP-ANSHIVTIFPDSSERYL 296
           L+  + DA A +R  A   G+ +G SSGA + A+LQ+A     A   IV + P  SERYL
Sbjct: 244 LSAYEEDAIAVIRTCAAREGIPLGVSSGAIVWAALQVAKRPENAGKRIVAVCPSGSERYL 303

Query: 297 SQKI 300
           S  +
Sbjct: 304 SSTL 307


Lambda     K      H
   0.317    0.133    0.378 

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: 244
Number of extensions: 12
Number of successful extensions: 3
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: 303
Length of database: 329
Length adjustment: 27
Effective length of query: 276
Effective length of database: 302
Effective search space:    83352
Effective search space used:    83352
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 (21.7 bits)
S2: 48 (23.1 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