GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metZ in Acidovorax sp. GW101-3H11

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate Ac3H11_34 Methionine gamma-lyase (EC 4.4.1.11)

Query= SwissProt::P9WGB5
         (406 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_34
          Length = 434

 Score =  263 bits (672), Expect = 7e-75
 Identities = 152/368 (41%), Positives = 220/368 (59%), Gaps = 6/368 (1%)

Query: 40  MYLTSGYVYGSAAVAEKSFAGELDHYVYSRYGNPTVSVFEERLRLIEGAPAAFATASGMA 99
           ++ ++ Y +   A   + FAG+   Y Y+R  NPT+++ E RL  +E    A    SGM 
Sbjct: 35  IHTSATYAFPDVAYGARCFAGQEPGYFYTRIANPTLALLEGRLAALEEGAGAVVFGSGMG 94

Query: 100 AVFTSLGALLGAGDRLVAARSLFGSCFVVCSEILPRWGVQTVFVDGDDLSQWERALSVPT 159
           A+  +L ++L  GD ++A  +L+G  F      L R+GV    VD  D ++   AL+  T
Sbjct: 95  AITATLWSMLEPGDEILADLTLYGCTFSFLHHGLGRFGVTVRHVDMTDPARVAEALTAKT 154

Query: 160 QAVFFETPSNPMQSLVDIAAVTELAHAAGAKVVLDNVFATPLLQQGFPLGVDVVVYSGTK 219
           + ++ ETP+NP   LVDIAAV+ LAHA GAKVV+DN + TP LQQ   LG DV V+S TK
Sbjct: 155 RVLYLETPANPNMRLVDIAAVSALAHAQGAKVVVDNTYCTPYLQQPLLLGADVSVHSMTK 214

Query: 220 HIDGQGRV-LGGAILGDREYIDG-PVQKLMRHTGPAMSAFNAWVLLKGLETLAIRVQHSN 277
           ++ G G +  G A+  D E      +  L   TG  MSA +A ++++GL+TLA+R+    
Sbjct: 215 YLGGHGDLTAGAAVFADAELAQRVRLYGLKDMTGAVMSAQDAHLVMRGLKTLALRMDRHC 274

Query: 278 ASAQRIAEFLNGHPSVRWVRYPYLPSHPQYDLAKRQMSGGGTVVTFALDCPEDVAKQRAF 337
            SAQ++AEF+  HP+   V YP LPS  Q+ LAK+QM   G ++ F L        Q   
Sbjct: 275 QSAQKVAEFIAAHPAAAAVHYPGLPSFAQHALAKQQMRQMGGMIAFEL----RGGLQAGV 330

Query: 338 EVLDKMRLIDISNNLGDAKSLVTHPATTTHRAMGPEGRAAIGLGDGVVRISVGLEDTDDL 397
             +D ++L+  + +LGDA++L  HPA+ TH    PE RAA G+ +G+VR+SVGLED DDL
Sbjct: 331 RFMDALQLVTRAVSLGDAETLAQHPASMTHSTYTPEQRAAHGIAEGLVRLSVGLEDLDDL 390

Query: 398 IADIDRAL 405
           +ADI +AL
Sbjct: 391 LADIGQAL 398


Lambda     K      H
   0.319    0.135    0.395 

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: 480
Number of extensions: 16
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: 406
Length of database: 434
Length adjustment: 32
Effective length of query: 374
Effective length of database: 402
Effective search space:   150348
Effective search space used:   150348
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