GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Pseudomonas stutzeri RCH2

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate GFF2528 Psest_2578 O-succinylhomoserine sulfhydrylase

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__psRCH2:GFF2528
          Length = 403

 Score =  315 bits (807), Expect = 1e-90
 Identities = 172/390 (44%), Positives = 250/390 (64%), Gaps = 13/390 (3%)

Query: 13  RALSLATLAIHGGQSPDPSTGAVMPPIYATSTYAQSSP--------GEHQGFEYSRTHNP 64
           + + L TLA+  GQ   P  G    P++ TS+Y   S         G+  G  YSR  NP
Sbjct: 15  QGVGLDTLAVRAGQRRTPE-GEHGEPLFFTSSYVFRSAADAAARFAGDVPGNVYSRYTNP 73

Query: 65  TRFAYERCVAALEGGTRAFAFASGMAAT-STVMELLDAGSHVVAMDDLYGGTFRLFERVR 123
           T  A+E  +AALEG  +A A ASGMAA  +TVM L  AG HV+    ++G T  LFE+  
Sbjct: 74  TVRAFEERIAALEGAEQAVATASGMAAILATVMSLCAAGDHVLVSRSVFGATVSLFEKYL 133

Query: 124 RRTAGLDFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTV 183
           +R  G+   +V LTD +A+++A + +TK+V++E+P+NP+ +LVDIAA+A +    G +  
Sbjct: 134 KRF-GVQVDYVPLTDFSAWESAFQENTKLVFVESPSNPLAELVDIAALAKLCHAKGAMLA 192

Query: 184 VDNTFASPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIG 243
           VDN F +P+LQ+PL+LGAD+V+HSATKY++G    +GG+ V G + ++ E + FL+ + G
Sbjct: 193 VDNCFCTPVLQQPLALGADIVIHSATKYIDGQGRCLGGV-VAGRSEQMKELVGFLRTA-G 250

Query: 244 GVQGPFDSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAK 303
               PF++++ L+GL+TL LRM+AHC +A  LA+WLE  P IE+V Y GL SHPQH LAK
Sbjct: 251 PTLSPFNAWVFLKGLETLRLRMQAHCASAQELAEWLEQQPGIERVYYAGLPSHPQHELAK 310

Query: 304 RQMSGFGGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARR 363
           RQ  GFG +VS  + GG +AA RF + T L ++  +LG  ++ + HP   TH  +    R
Sbjct: 311 RQQKGFGAVVSFEVAGGKEAAWRFIDATRLISITANLGDSKTTITHPGSTTHGRLSAEDR 370

Query: 364 EQLGISDALVRLSVGIEDLGDLRGDLERAL 393
              GI D+L+R++VG+ED+ DL+ DL R L
Sbjct: 371 ATAGIRDSLIRVAVGLEDVADLKADLARGL 400


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: 430
Number of extensions: 22
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: 403
Length adjustment: 31
Effective length of query: 366
Effective length of database: 372
Effective search space:   136152
Effective search space used:   136152
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