GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Thiothrix lacustris DSM 21227

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_028489058.1 Q394_RS0109350 alanine transaminase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000621325.1:WP_028489058.1
          Length = 397

 Score =  350 bits (898), Expect = e-101
 Identities = 173/381 (45%), Positives = 247/381 (64%), Gaps = 3/381 (0%)

Query: 11  RIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHGYP 70
           RI +LP YVF   D LK +AR +G D+ID GMGNPD  TP+ +VD  ++A Q    H Y 
Sbjct: 7   RINRLPTYVFKITDALKREARAKGEDIIDFGMGNPDQPTPKHIVDKLVEAAQRGDTHRYS 66

Query: 71  PFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPSPA 130
              G    R+AI+NWY R++ V +DP++EA+  +GSKEGL+HLA+A ++ GD VLVP+PA
Sbjct: 67  MSRGIPRLRKAISNWYKRKFDVDIDPETEAIVTIGSKEGLAHLALATLSRGDTVLVPNPA 126

Query: 131 YPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAPRE 190
           YP H  G +IA   +  + L    D+  +L A  +    K K+L  N+P+NPTG     E
Sbjct: 127 YPIHPYGSIIADADIRHVPLVEGKDFFEELEAAIKNSWPKPKMLIINFPANPTGQCVDLE 186

Query: 191 FFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMAGW 250
           FFE ++  A+++++ ++HD+ Y E+ FDGY+  S+L++PGAKDI VEF++LSKTYNM GW
Sbjct: 187 FFERVIKVAKEHDVWVIHDIAYGEICFDGYEAPSILQVPGAKDIAVEFYSLSKTYNMPGW 246

Query: 251 RVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDFLI 310
           RVGF+ GN  +++ L  +K+ LDYG+FA +Q AA  AL+ P   + E+   Y +RR+ L 
Sbjct: 247 RVGFMCGNPVLVKALERIKSYLDYGMFAPIQIAAIAALEGPQDCVKEISAMYESRRNVLC 306

Query: 311 QGLGELGWDVPKTKATMYLWVKCP---VGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGY 367
            GL   GW V + KA+M++W K P     MGS +FA  LL++  V V+PG  FG  G+ +
Sbjct: 307 DGLNAAGWAVERPKASMFVWAKIPEHYAAMGSLEFAKKLLKEAQVAVSPGIGFGEYGDDH 366

Query: 368 VRISLIADCDRLGEALDRIKQ 388
           VR SLI +  R  +A+  IKQ
Sbjct: 367 VRFSLIENEHRTRQAIRNIKQ 387


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: 461
Number of extensions: 21
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: 397
Length adjustment: 31
Effective length of query: 372
Effective length of database: 366
Effective search space:   136152
Effective search space used:   136152
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 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