GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Desulfacinum hydrothermale DSM 13146

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_084057643.1 B9A12_RS09460 alanine transaminase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_900176285.1:WP_084057643.1
          Length = 395

 Score =  345 bits (885), Expect = 1e-99
 Identities = 169/382 (44%), Positives = 248/382 (64%), Gaps = 3/382 (0%)

Query: 11  RIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHGYP 70
           R+++LPPYVFA+++ LK + R  G D++DLGMGNPD  TP  +V+  ++A +   NH Y 
Sbjct: 10  RMRRLPPYVFAQVNALKMERRRAGEDIVDLGMGNPDLPTPPHIVEKLVEAARKGHNHRYS 69

Query: 71  PFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPSPA 130
             +G    R AI +WY RRY V LDP+SEA+  +G+KEGLSHL +A V+PGDVV  P+P 
Sbjct: 70  ASKGITKLRHAICDWYKRRYQVDLDPESEAVVTIGAKEGLSHLVLALVSPGDVVFSPNPT 129

Query: 131 YPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAPRE 190
           YP H    +IAGG + S+ + P  D+  DL    ++   + K+L  ++P NPT A    +
Sbjct: 130 YPIHPYSVIIAGGDLRSIPIGPGRDFFEDLLIATKQTWPRPKMLIISFPHNPTTAVVDMD 189

Query: 191 FFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMAGW 250
           FF+++V FAR   ++++HDL YA+L FDGY+  S+L++PGAKD+ VEF ++SK+Y+MAGW
Sbjct: 190 FFQKVVDFARDNHLMVIHDLAYADLTFDGYRAPSILQVPGAKDVAVEFFSMSKSYSMAGW 249

Query: 251 RVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDFLI 310
           RVGF VGN  ++  L  LK+ LDYGIF  +Q AA  AL      + E+   Y++RRD L+
Sbjct: 250 RVGFCVGNPEMVAALTRLKSYLDYGIFQPIQIAAIIALNGDQSCVQEIVDIYQSRRDVLV 309

Query: 311 QGLGELGWDVPKTKATMYLWVKCPV---GMGSTDFALNLLQQTGVVVTPGNAFGVAGEGY 367
            GL   GW + K K TM++W   P     MGS  F+  L+++  V V+PG  FG  G+ +
Sbjct: 310 DGLNRAGWPLEKPKGTMFVWAPIPEAFRSMGSVAFSKFLIEKAKVAVSPGLGFGEYGDDH 369

Query: 368 VRISLIADCDRLGEALDRIKQA 389
           VR +L+ +  R+ +A+  I++A
Sbjct: 370 VRFALVENEMRIRQAVRGIRKA 391


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: 465
Number of extensions: 23
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: 395
Length adjustment: 31
Effective length of query: 372
Effective length of database: 364
Effective search space:   135408
Effective search space used:   135408
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