GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Shewanella loihica PV-4

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate 5210044 Shew_2491 methionine gamma-lyase (RefSeq)

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__PV4:5210044
          Length = 391

 Score =  313 bits (803), Expect = 4e-90
 Identities = 172/385 (44%), Positives = 239/385 (62%), Gaps = 12/385 (3%)

Query: 17  LATLAIHGGQSPDPSTGAVMPPIYATSTYAQSS--------PGEHQGFEYSRTHNPTRFA 68
           LAT  IH G   +   GA++ P+  ++T+   +         GE QG+ Y+R  NPT   
Sbjct: 7   LATQVIHAGHEANQH-GALVSPLVQSATFTFETVEQGGDCFAGEQQGYIYTRLGNPTTAE 65

Query: 69  YERCVAALEGGTRAFAFASGMAATST-VMELLDAGSHVVAMDDLYGGTFRLFERVRRRTA 127
            ER +A LEG   A A ASGMAA S  ++  L  G H+VA   +YG TF L     +R  
Sbjct: 66  LERKMAVLEGSEAAAATASGMAAVSAALLTNLSQGDHLVASKAVYGCTFALMTEQFKRF- 124

Query: 128 GLDFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNT 187
           G++ + VD  + A    AIR +TK ++ ETP NP L + D+AAIA +A++H L+++VDNT
Sbjct: 125 GIEVTLVDFCEVANIAQAIRPNTKALFCETPVNPHLDVYDLAAIAALAKRHQLVSIVDNT 184

Query: 188 FASPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQG 247
           F +P+LQRPLS+G D+V+HSATKYLNGH D++ GI V G    + +    +   IGGV  
Sbjct: 185 FMTPLLQRPLSMGIDMVIHSATKYLNGHGDVIAGI-VCGTEEMITKVKLEVLKDIGGVIS 243

Query: 248 PFDSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMS 307
           P D++L LRGLKTL +R+  HC+NA  +A++L+ HP + +V YPGL  H  H L  +QM 
Sbjct: 244 PHDAWLILRGLKTLDVRLARHCDNAERVAEYLQQHPQVARVYYPGLKGHSGHALLGKQML 303

Query: 308 GFGGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLG 367
             GG+V+  LKG FDAAK F  + +LF +A SLG  ESL+ HPA MTH+      R   G
Sbjct: 304 RAGGVVAFELKGSFDAAKAFANRLKLFKIAVSLGDAESLIQHPASMTHSPYSPEARMDAG 363

Query: 368 ISDALVRLSVGIEDLGDLRGDLERA 392
           I D+L+R+S+G+ED  D+  DL +A
Sbjct: 364 IGDSLLRISLGLEDSDDIIADLAQA 388


Lambda     K      H
   0.320    0.134    0.391 

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: 429
Number of extensions: 17
Number of successful extensions: 4
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: 397
Length of database: 391
Length adjustment: 31
Effective length of query: 366
Effective length of database: 360
Effective search space:   131760
Effective search space used:   131760
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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