GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Phaeobacter inhibens BS107

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate GFF2323 PGA1_c23540 O-succinylhomoserine sulfhydrylase MetZ

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__Phaeo:GFF2323
          Length = 396

 Score =  265 bits (677), Expect = 2e-75
 Identities = 147/355 (41%), Positives = 220/355 (61%), Gaps = 7/355 (1%)

Query: 41  ATSTYAQSSPGEHQGFEYSRTHNPTRFAYERCVAALEGGTRAFAFASGMAATSTVM-ELL 99
           A + + ++ P E   F Y+R  NPT   +E  +AALEG   AFA ASGMAA +  +  +L
Sbjct: 42  AEARFIETGPDE---FIYARYGNPTVAMFEERIAALEGAEDAFATASGMAAVNGALTSIL 98

Query: 100 DAGSHVVAMDDLYGGTFRLFERVRRRTAGLDFSFVDLTDPAAFKAAIRADTKMVWIETPT 159
            AG HVV+   L+G    + E +  R  G++ +FVD TD  A++AA+R DTK V+ E+ +
Sbjct: 99  KAGDHVVSAKALFGSCLYILENILTRY-GVEVTFVDGTDLDAWRAALRPDTKAVFFESMS 157

Query: 160 NPMLKLVDIAAIAVIARKHGLLTVVDNTFASPMLQRPLSLGADLVVHSATKYLNGHSDMV 219
           NP L+++DIAA+A +A   G   VVDN F++P+    +  GAD+V++SATK+++G   ++
Sbjct: 158 NPTLEVIDIAAVAELAHAVGATVVVDNVFSTPVFSNAIEQGADVVIYSATKHIDGQGRVL 217

Query: 220 GGIAVVGDNAELAEQMAFLQNSIGGVQGPFDSFLALRGLKTLPLRMRAHCENALALAQWL 279
           GG+ ++G    +   +       GG   PF+++  L+GL+T+ LR+ A  E AL LAQ L
Sbjct: 218 GGV-ILGTRDFIRGTVEPYMKHTGGSLSPFNAWTLLKGLETISLRVNAQAETALELAQAL 276

Query: 280 ETHPAIEKVIYPGLASHPQHVLAKRQMSGFGG-IVSIVLKGGFDAAKRFCEKTELFTLAE 338
             HPA+ +++YPGL  H QH L +RQ+ G GG ++S+ LKGG DAA RF     +  ++ 
Sbjct: 277 SGHPALSRLMYPGLEDHAQHALVQRQLGGKGGTVLSLDLKGGKDAAFRFLNALTIPVISN 336

Query: 339 SLGGVESLVNHPAVMTHASIPVARREQLGISDALVRLSVGIEDLGDLRGDLERAL 393
           +LG  +S+  HPA  TH  +    + +LGI+  LVR SVG+ED GDL  DL +AL
Sbjct: 337 NLGDAKSIATHPATTTHQRLSEELKSELGITPGLVRFSVGLEDAGDLIADLTQAL 391


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: 434
Number of extensions: 24
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: 397
Length of database: 396
Length adjustment: 31
Effective length of query: 366
Effective length of database: 365
Effective search space:   133590
Effective search space used:   133590
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