GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Desulfovibrio oxyclinae DSM 11498

Align Putative [LysW]-L-2-aminoadipate/[LysW]-L-glutamate phosphate reductase; EC 1.2.1.103; EC 1.2.1.106 (uncharacterized)
to candidate WP_018125987.1 B149_RS0114990 N-acetyl-gamma-glutamyl-phosphate reductase

Query= curated2:A0RWW0
         (348 letters)



>NCBI__GCF_000375485.1:WP_018125987.1
          Length = 351

 Score =  264 bits (675), Expect = 2e-75
 Identities = 141/348 (40%), Positives = 207/348 (59%), Gaps = 8/348 (2%)

Query: 4   GVVGASGYVGGETLRLLVNHPDVEIAAVTSRQHVGEYLHRVQPSLRGFT--DLTFSELDY 61
           G+VG +GY G E  RL+ +HP +E+  VTSR   G+ L  + P L+G    +L  +E D 
Sbjct: 8   GLVGVTGYAGMELARLMTSHPSMELVRVTSRAEAGKKLSDLYPFLQGLGPGELEVTEPDP 67

Query: 62  DRLSDSCDLVFTAVPHGTATDIVRALYDRDIKVIDLSADYRLHDPADYTKWYGWEHPHPD 121
             L+ SCD+VF AVPH  A +I   L +  +KV+DLSAD+RL D   Y +WY   H  P+
Sbjct: 68  RDLATSCDVVFLAVPHKAAMEIAAVLLEEGVKVVDLSADFRLRDRCTYEQWYDVPHTRPE 127

Query: 122 YLSKSVFGIPELHREEIRSAKLVSCPGCMAVTSILALAPPVREGLVDTEHIVVDSKIGSS 181
            L ++V+G+PEL+ + I  A L++ PGC    S+L LAP ++ GLV+T+ +++D+K G+S
Sbjct: 128 LLEQAVYGLPELYADRIPLANLIANPGCYPTASVLGLAPALKNGLVETDGVIIDAKSGAS 187

Query: 182 GAGAGAGTAHAMRA--GVIRPYKPAKHRHTGEIEQELSGIAGKKIRVSMSPHAVDVVRGI 239
           GAG GA   +         R Y   KHRHT EIEQE   +AG  + +S + H + + RGI
Sbjct: 188 GAGRGAKVPNLFCEVHDSFRAYGLPKHRHTPEIEQEAGLLAGTDMVLSFNTHLLPIDRGI 247

Query: 240 LCTNHVFLTREASEKDLWKMYRQAYGEERFVRLIRDKKGLYKFPDPKFLVGSNFCDIGFD 299
           L T +  L    + + + + Y   Y ++ +VR++ +     KFP+ +F+ G+ FCDIG  
Sbjct: 248 LATIYTSLKDGVTMEAVREAYESFYADKPYVRVLPEG----KFPETRFVRGTMFCDIGLV 303

Query: 300 LDEDNNRLVAISASDNLMKGAAGSAIQNMNIMAGLDEMSGLRYTPLTP 347
            D    RL+ +SA DNL +GA+G A+ N N+M GLD   GL   PL P
Sbjct: 304 TDPRTGRLIILSAIDNLCRGASGQALANANLMCGLDISLGLPTAPLMP 351


Lambda     K      H
   0.320    0.137    0.412 

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: 277
Number of extensions: 10
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: 348
Length of database: 351
Length adjustment: 29
Effective length of query: 319
Effective length of database: 322
Effective search space:   102718
Effective search space used:   102718
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: 49 (23.5 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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