GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Pseudomonas putida KT2440

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate PP_2001 PP_2001 O-succinylhomoserine sulfhydrylase

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__Putida:PP_2001
          Length = 403

 Score =  308 bits (788), Expect = 2e-88
 Identities = 167/384 (43%), Positives = 245/384 (63%), Gaps = 13/384 (3%)

Query: 19  TLAIHGGQSPDPSTGAVMPPIYATSTY--------AQSSPGEHQGFEYSRTHNPTRFAYE 70
           TLA+  GQ+  P  G     ++ TS+Y        A    GE  G  YSR  NP+  A+E
Sbjct: 21  TLAVRAGQNRTPE-GEHSEALFLTSSYVFRTAADAAARFAGETPGNVYSRYTNPSVRAFE 79

Query: 71  RCVAALEGGTRAFAFASGMAAT-STVMELLDAGSHVVAMDDLYGGTFRLFERVRRRTAGL 129
             +AA+EG  +A   ++GMAA  + VM L  AG HV+    ++G T  LFE+  +R  G+
Sbjct: 80  ERLAAMEGAEQAVGTSTGMAAILAVVMSLCSAGDHVLVSQSVFGSTISLFEKYFKRF-GV 138

Query: 130 DFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNTFA 189
           +  +V L D   ++ AI+A+TK++ +E+P+NP+ +LVDI A++ IA   G + VVDN F+
Sbjct: 139 EVDYVPLVDLTGWEKAIKANTKLLIVESPSNPLAELVDITALSEIAHAQGAMLVVDNCFS 198

Query: 190 SPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQGPF 249
           +P LQ+PL LGAD+V HSATK+++G    +GG+ V G   ++ E + FL+ + G    PF
Sbjct: 199 TPALQQPLKLGADIVFHSATKFIDGQGRCMGGV-VAGRTEQMKEVVGFLRTA-GPTLSPF 256

Query: 250 DSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMSGF 309
           ++++  +GL+TL LRMRAHCE+A ALA+WLE    +EKV Y GL SHPQH LAKRQMSGF
Sbjct: 257 NAWIFTKGLETLRLRMRAHCESAQALAEWLEQQDGVEKVHYAGLPSHPQHELAKRQMSGF 316

Query: 310 GGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLGIS 369
           G +VS  +KGG + A RF + T + ++  +LG  ++ + HPA  +H  +    RE  GI 
Sbjct: 317 GAVVSFEVKGGKEGAWRFIDATRVISITTNLGDSKTTIAHPATTSHGRLSPQEREAAGIR 376

Query: 370 DALVRLSVGIEDLGDLRGDLERAL 393
           D+L+R++VG+ED+ DL+ DL R L
Sbjct: 377 DSLIRVAVGLEDVADLQADLARGL 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: 413
Number of extensions: 18
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