GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Dehalococcoides mccartyi 195

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_010936475.1 DET_RS03860 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000011905.1:WP_010936475.1
          Length = 388

 Score =  358 bits (920), Expect = e-103
 Identities = 172/376 (45%), Positives = 246/376 (65%)

Query: 11  RIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHGYP 70
           RI+ LPPY+F ++ +  A+ R +G ++I   +G+PD  TP+ ++    +A +DP NH YP
Sbjct: 6   RIENLPPYLFVQISKKIAEKRAKGEEVISFAIGDPDLPTPKHILAELCKAAEDPANHRYP 65

Query: 71  PFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPSPA 130
             EG    R+A+  WY +R+GV L+PD+E LPL+GSKEG+ H A  +++PGDV LVP PA
Sbjct: 66  ETEGLPVLRKAMAEWYEKRFGVKLNPDTEVLPLIGSKEGIGHAAWCFLDPGDVALVPDPA 125

Query: 131 YPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAPRE 190
           YP +     +AG  V  + L  EN++L D  AIP++V  KAKIL+ NYP+NPTGA A  +
Sbjct: 126 YPVYAISSQLAGAEVFYMPLNKENNFLPDFNAIPQDVLSKAKILWINYPNNPTGAVAGLD 185

Query: 191 FFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMAGW 250
           FF+E   FA K+ + + HD  Y+E+AFDGY+P S LE  GAK++G+EFH+LSK+YNM GW
Sbjct: 186 FFKEAAEFAAKHNLAVCHDGPYSEIAFDGYRPVSFLEADGAKEVGIEFHSLSKSYNMTGW 245

Query: 251 RVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDFLI 310
           R+G  VGN  +I  LR  K+NLD GI  A+Q  A  AL      + +    Y+ RRD L+
Sbjct: 246 RIGMAVGNAKMIDALRRFKSNLDSGIPQAIQLMAIAALNGSQDVISQNCAVYQRRRDRLV 305

Query: 311 QGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGYVRI 370
           + L  +G +V   KA++Y+W   P G  S  FA  LL +TGVVVTPG  +G +GEGY+R+
Sbjct: 306 EALRNIGMEVTAPKASLYIWAPVPEGYTSASFATELLDKTGVVVTPGTGYGTSGEGYIRL 365

Query: 371 SLIADCDRLGEALDRI 386
           SL    ++L + + ++
Sbjct: 366 SLTVPDEQLEKGIAKL 381


Lambda     K      H
   0.321    0.140    0.427 

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: 488
Number of extensions: 19
Number of successful extensions: 2
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: 388
Length adjustment: 31
Effective length of query: 372
Effective length of database: 357
Effective search space:   132804
Effective search space used:   132804
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.

Links

Downloads

Related tools

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