GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metZ in Pseudomonas fluorescens FW300-N2E3

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate AO353_24330 AO353_24330 cystathionine beta-lyase

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_24330
          Length = 389

 Score =  177 bits (448), Expect = 6e-49
 Identities = 111/338 (32%), Positives = 172/338 (50%), Gaps = 10/338 (2%)

Query: 67  YSRYTNPTVRTFEERIAALEGAEQAVATASGMSAILALVMSLCSSGDHVLVSRSVFGSTI 126
           Y R+ NP+     + +  LEGAE  V   SG+SA    ++S+  +GDH+L++ +V+    
Sbjct: 52  YGRWNNPSTEALTQALQQLEGAEGTVLCPSGLSACTTAILSVVGAGDHLLIADNVYSPIR 111

Query: 127 SLFDKYFKRFGIQVDYPPLSDLAAWEAACKPNTKLFFVESPSNPLAELVDIAALAEIAHA 186
           +  ++  +R GI+V +   +  A      KPNTK  + ESP +   E+ DI A+A++AH 
Sbjct: 112 AFCEQVGQRLGIEVTFYDPTIGAGIVDFLKPNTKAIYTESPGSLTLEIQDIPAIAKVAHE 171

Query: 187 KGALLAVDNCFCTPALQQPLKLGADVVIHSATKYIDGQGRGMGGVVAGRGEQMKEVVGFL 246
              L+  DN + TP     L+LG D+ I +ATKYI G    + G V+        +  F 
Sbjct: 172 HDILVITDNTWGTPLYFPSLELGVDLSIMAATKYIVGHSDAVLGTVSASKRAWDSLKRFH 231

Query: 247 RTAGPTLSPFNAWLFLKGLETLRIRMQAHSASALALAEWLERQPGIERVYYAGLPSHPQH 306
              G   SP +  L L+G+ TL +R++ H  +A  +A+WLE +  +E VYY  L SHPQH
Sbjct: 232 FNMGLFASPDDVTLALRGMRTLDVRLERHYKNATTVAKWLETREEVEAVYYPALESHPQH 291

Query: 307 ELARRQQSGFGAVVSFDVKGGRDAAW-RFIDATRMVSITTNLG--DTKTTIAHPATTSHG 363
           +L +R   G   ++SF  K    AA    +D+  + SI  + G  ++   IA P      
Sbjct: 292 QLWKRDFKGASGLLSFVTKPSTQAAADALLDSLSLFSIGYSWGGFESLAMIADPKPV--- 348

Query: 364 RLSPEDRARAGIGDSLIRVAVGLEDLDDLKADMARGLA 401
                      I   L+R+ +GLED  DL  D+ +G A
Sbjct: 349 ----RSATSWEIDGHLVRLHIGLEDPSDLIEDLEQGFA 382


Lambda     K      H
   0.319    0.133    0.392 

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: 340
Number of extensions: 19
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: 403
Length of database: 389
Length adjustment: 31
Effective length of query: 372
Effective length of database: 358
Effective search space:   133176
Effective search space used:   133176
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