GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metZ in Pseudomonas fluorescens FW300-N2E2

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate Pf6N2E2_1491 Cystathionine beta-lyase (EC 4.4.1.8)

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1491
          Length = 921

 Score =  193 bits (491), Expect = 2e-53
 Identities = 118/338 (34%), Positives = 182/338 (53%), Gaps = 12/338 (3%)

Query: 67  YSRYTNPTVRTFEERIAALEGAEQAVATASGMSAILALVMSLCSSGDHVLVSRSVFGSTI 126
           Y    NPT    E+ +  LEG  +     +G++A+    ++    GDHVL++ +V+    
Sbjct: 584 YGARGNPTAFALEDLVTELEGGYRTRLFGTGLAAVAQTFLTYLRPGDHVLITDAVYAPVR 643

Query: 127 SLFDKYFKRFGIQVDY--PPLSDLAAWEAACKPNTKLFFVESPSNPLAELVDIAALAEIA 184
            +   + + FGIQV Y  P  SDL       + NTK+ + E P + L EL D+ A+A + 
Sbjct: 644 RVARDFLEAFGIQVGYFAPDGSDLPG---RLQANTKMVYTEVPGSLLYELCDLPAIAALC 700

Query: 185 HAKGALLAVDNCFCTPALQQPLKLGADVVIHSATKYIDGQGRGMGGVVAGRGEQMKEVVG 244
             +G LLAVDN + +  L +PL LGAD+ I + TKY+ G    + G V  R E    +  
Sbjct: 701 KPRGILLAVDNTWGSGVLYRPLTLGADISIMALTKYLSGHSDVLMGSVCTRQEAWPALAA 760

Query: 245 FLRTAGPTLSPFNAWLFLKGLETLRIRMQAHSASALALAEWLERQPGIERVYYAGLPSHP 304
              T G T+SP +A+L L+G  TL  R+  H   AL +A WL+ QP ++RV++  LP HP
Sbjct: 761 MSDTFGNTVSPDDAYLVLRGARTLMPRLDTHERQALEVARWLQAQPQVKRVFHPALPEHP 820

Query: 305 QHELARRQQSGFGAVVSFDVKGGRDA-AWRFIDATRMVSITTNLGDTKTTIAHPATTSHG 363
           +H L +R   G   ++SF+++   DA   RFIDA ++  +  + G  ++ +      +  
Sbjct: 821 RHALWQRDFKGSNGLLSFELRENDDAYLERFIDALQVFGLGASWGGFESLVT--VADTKD 878

Query: 364 RLSPEDRARAGIGDSLIRVAVGLEDLDDLKADMARGLA 401
           R S EDRA     + ++R+ VGLED+D L  D+ RG A
Sbjct: 879 RQSAEDRAL----NPVVRLHVGLEDVDVLVEDLRRGFA 912


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: 809
Number of extensions: 42
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: 921
Length adjustment: 37
Effective length of query: 366
Effective length of database: 884
Effective search space:   323544
Effective search space used:   323544
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: 53 (25.0 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