GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysN in Sulfurimonas denitrificans DSM 1251

Align 2-aminoadipate transaminase; 2-aminoadipate aminotransferase; L-2AA aminotransferase; EC 2.6.1.39 (characterized)
to candidate WP_011372739.1 SUDEN_RS05820 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::Q88FI7
         (416 letters)



>NCBI__GCF_000012965.1:WP_011372739.1
          Length = 430

 Score =  132 bits (331), Expect = 3e-35
 Identities = 100/332 (30%), Positives = 152/332 (45%), Gaps = 24/332 (7%)

Query: 15  PITLSHGRNAEVWDTDGKRYIDFVGGIGVLNLGHCNPAVVEAIQAQATRLTHYAFNAAPH 74
           P+ +++G  A + D DG RY+DFV   G L  GH + ++  A+         +       
Sbjct: 35  PLFIANGSGAYLTDIDGNRYVDFVQSWGPLLFGHRDESIESAVIEAVKHGLSFGAPTQAE 94

Query: 75  GPYLALMEQLSQFVPVSYPLAGMLTNSGAEAAENALKVARGATGKRAIIAFDGGFHGRTL 134
               AL+  +S F  +         +SG EA  +A+++ARG T    I+ F G +HG + 
Sbjct: 95  SDLAALV--ISMFDSIEKI---RFVSSGTEAVMSAIRLARGYTNCDDIVKFTGCYHGHSD 149

Query: 135 ATLNLNGKVAPYKQRVGELPGPVYHLPYPSADTGVTCEQALKAMDRLFSVELAV---EDV 191
           + L   G  A                  P      T    L   + + SV+      +DV
Sbjct: 150 SLLVQAGSGAATFGNPSS----------PGVPADFTKHTLLAEYNNIESVKKCFSDSKDV 199

Query: 192 AAFIFEPVQGEGGFLALDPAFAQALRRFCDERGILIIIDEIQSGFGRTGQRFAFPRLGIE 251
           A  I EP+ G  G +  D  F + LR  CD  G L+I DE+ SGF R     A    G++
Sbjct: 200 ACVIIEPIAGNMGLVPADKEFLRELRELCDANGALLIFDEVMSGF-RASVHGAESITGVK 258

Query: 252 PDLLLLAKSIAGGMPLGAVVGRKELMAAL-PKGGL--GGTYSGNPISCAAALASLAQMTD 308
           PD++ L K I GGMP+GA   R E+MA L P+G +   GT SGNP++ AA LA++ ++  
Sbjct: 259 PDIVTLGKVIGGGMPVGAFGARAEIMAKLSPEGPVYQAGTLSGNPVAMAAGLAAITKLKQ 318

Query: 309 EN--LATWGERQEQAIVSRYERWKASGLSPYI 338
               ++    R  + +    E  K  G++  I
Sbjct: 319 NGQIISVLNSRATRLVEGMQEAAKTYGIAMQI 350


Lambda     K      H
   0.320    0.137    0.402 

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: 405
Number of extensions: 26
Number of successful extensions: 5
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: 416
Length of database: 430
Length adjustment: 32
Effective length of query: 384
Effective length of database: 398
Effective search space:   152832
Effective search space used:   152832
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 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