GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Dehalococcoides mccartyi 195

Align alanine-glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate WP_010936475.1 DET_RS03860 diaminopimelate aminotransferase

Query= BRENDA::D2Z0I0
         (402 letters)



>NCBI__GCF_000011905.1:WP_010936475.1
          Length = 388

 Score =  296 bits (758), Expect = 7e-85
 Identities = 138/379 (36%), Positives = 231/379 (60%), Gaps = 6/379 (1%)

Query: 9   KVKKLPKYVFAMVNELKYQLRREGEDIVDLGMGNPDIPPSQHIIDKLCEVANRPNVHGYS 68
           +++ LP Y+F  +++   + R +GE+++   +G+PD+P  +HI+ +LC+ A  P  H Y 
Sbjct: 6   RIENLPPYLFVQISKKIAEKRAKGEEVISFAIGDPDLPTPKHILAELCKAAEDPANHRYP 65

Query: 69  ASKGIPRLRKAICDFYKRRYGVELDPERNAIMTIGAKEGYSHLMLAMLEPGDTVIVPNPT 128
            ++G+P LRKA+ ++Y++R+GV+L+P+   +  IG+KEG  H     L+PGD  +VP+P 
Sbjct: 66  ETEGLPVLRKAMAEWYEKRFGVKLNPDTEVLPLIGSKEGIGHAAWCFLDPGDVALVPDPA 125

Query: 129 YPIHYYAPIICGGDAISVPILPEEDFPEVFLRRLYDLIKTSFRKPKAVVLSFPHNPTTLC 188
           YP++  +  + G +   +P+  E +F   F     D++     K K + +++P+NPT   
Sbjct: 126 YPVYAISSQLAGAEVFYMPLNKENNFLPDFNAIPQDVLS----KAKILWINYPNNPTGAV 181

Query: 189 VDLEFFQEVVKLAKQEGIWIVHDFAYADLGFDGYTPPSILQVEGALDVAVELYSMSKGFS 248
             L+FF+E  + A +  + + HD  Y+++ FDGY P S L+ +GA +V +E +S+SK ++
Sbjct: 182 AGLDFFKEAAEFAAKHNLAVCHDGPYSEIAFDGYRPVSFLEADGAKEVGIEFHSLSKSYN 241

Query: 249 MAGWRVAFVVGNEMLIKNLAHLKSYLDYGVFTPIQVASIIALESPYEVVEKNREIYRRRR 308
           M GWR+   VGN  +I  L   KS LD G+   IQ+ +I AL    +V+ +N  +Y+RRR
Sbjct: 242 MTGWRIGMAVGNAKMIDALRRFKSNLDSGIPQAIQLMAIAALNGSQDVISQNCAVYQRRR 301

Query: 309 DVLVEGLNRVGWEVKKPKGSMFVWAKVPEEVGMNSLDFSLFLLREAKVAVSPGIGFGEYG 368
           D LVE L  +G EV  PK S+++WA VPE  G  S  F+  LL +  V V+PG G+G  G
Sbjct: 302 DRLVEALRNIGMEVTAPKASLYIWAPVPE--GYTSASFATELLDKTGVVVTPGTGYGTSG 359

Query: 369 EGYVRFALVENEHRIRQAV 387
           EGY+R +L   + ++ + +
Sbjct: 360 EGYIRLSLTVPDEQLEKGI 378


Lambda     K      H
   0.322    0.141    0.425 

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: 427
Number of extensions: 18
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: 402
Length of database: 388
Length adjustment: 31
Effective length of query: 371
Effective length of database: 357
Effective search space:   132447
Effective search space used:   132447
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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