GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Allochromatium vinosum DSM 180

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_012971318.1 ALVIN_RS10590 alanine transaminase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000025485.1:WP_012971318.1
          Length = 400

 Score =  354 bits (908), Expect = e-102
 Identities = 179/381 (46%), Positives = 245/381 (64%), Gaps = 3/381 (0%)

Query: 11  RIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHGYP 70
           RI++LPPYVF  ++ELKA+AR +G D+ID GMGNPD  TPQ +VD  +++ Q P  H Y 
Sbjct: 10  RIKRLPPYVFNIVNELKAEARARGEDIIDFGMGNPDQGTPQHIVDKLVESAQRPDTHRYS 69

Query: 71  PFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPSPA 130
              G    RRA+ NWY  R+ V LDP+SEA+  +GSKEGL+HLA+A +  GD VLVP+PA
Sbjct: 70  MSRGIPRLRRAVCNWYRDRFDVHLDPESEAILTIGSKEGLAHLALATMGAGDTVLVPNPA 129

Query: 131 YPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAPRE 190
           YP H  G +IAG  V  + L P+ D+  +L    ++   K K+L  N+P NPT      +
Sbjct: 130 YPIHPYGFIIAGADVRHVRLTPDVDFFDELQKAIQDSWPKPKMLVLNFPGNPTTQCVELD 189

Query: 191 FFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMAGW 250
           FF++++  AR++ I +VHDL Y ++AFDGY+P S+L+IP AKDI VEF TLSK+YNM GW
Sbjct: 190 FFQKVIDIAREHGIWVVHDLAYVDIAFDGYKPPSILQIPEAKDIAVEFFTLSKSYNMPGW 249

Query: 251 RVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDFLI 310
           RVGF+ GN+ ++  L  +K+ LDYG F  +Q AA  AL+ P   + E+   Y++RRD L 
Sbjct: 250 RVGFMCGNKTLVSALARIKSYLDYGTFTPIQVAAIAALEGPQECVREISDMYQSRRDVLC 309

Query: 311 QGLGELGWDVPKTKATMYLWVKCPV---GMGSTDFALNLLQQTGVVVTPGNAFGVAGEGY 367
            GL   GW V   KATM++W   P     MGS +F+  LL+   V V PG  FG  G+ +
Sbjct: 310 AGLNAAGWPVEPPKATMFVWAPIPEPYRAMGSLEFSKKLLRDAKVAVAPGIGFGEYGDTH 369

Query: 368 VRISLIADCDRLGEALDRIKQ 388
           VR  LI +  R  +A+  IK+
Sbjct: 370 VRFGLIENEHRTRQAIRGIKE 390


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: 514
Number of extensions: 24
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: 400
Length adjustment: 31
Effective length of query: 372
Effective length of database: 369
Effective search space:   137268
Effective search space used:   137268
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