GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Thermovibrio ammonificans HB-1

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_013537347.1 THEAM_RS02990 succinyldiaminopimelate transaminase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000185805.1:WP_013537347.1
          Length = 387

 Score =  234 bits (597), Expect = 3e-66
 Identities = 133/382 (34%), Positives = 215/382 (56%), Gaps = 12/382 (3%)

Query: 12  IQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHGYPP 71
           I++L  Y   RL+  K + + +G+ L D G G+P   TP  + +A I+A+  P+   YP 
Sbjct: 5   IRELKSYPMDRLNRAKEEIKRKGLKLFDFGTGDPKEPTPSFIREALIRAV--PEVSQYPT 62

Query: 72  FEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGD---VVLVPS 128
            +G    R A   W  RR+GV L+P++E +P  GSKE + HL + ++        V+  +
Sbjct: 63  VKGRKELREAAAGWVKRRFGVELNPEAEVIPTAGSKEAIFHLPLVFIEAESDKRKVVFGT 122

Query: 129 PAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAP 188
           PAYP + RG + AGG  H + LK E ++L+ L  +P  +  + +I++ NYP NPTGA+AP
Sbjct: 123 PAYPVYLRGTLFAGGEPHPVELKFEENFLLRLDKLPRSLLEETRIVWINYPHNPTGASAP 182

Query: 189 REFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMA 248
             +FEE+    R++ I+L  D CY ++ F    P S+L++   K+  + FH+LSK   M 
Sbjct: 183 LSYFEEVYGICREHGIILCSDECYVDIYFT-EPPPSVLQV--GKEGVLAFHSLSKRSGMT 239

Query: 249 GWRVGFVVGNRHVIQGLRTLKTNLDYGIFAA-LQTAAETALQLPDIYLHEVQQRYRTRRD 307
           G+R GFV G+  ++Q    LK    +G+ +     AA TA    D ++ E ++ ++ +  
Sbjct: 240 GYRSGFVAGDGKLVQ--EYLKYRSSFGVASQDFVQAAATAAWSDDGHVEERRRIFKEKAK 297

Query: 308 FLIQGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGY 367
              +   E+G +    +AT YLWVK P G+    +AL+LL+  G+VV+PG  FG  GEG+
Sbjct: 298 VFSEFFKEIGLEFLPAEATFYLWVKTPKGVSGEKYALHLLKY-GIVVSPGEFFGRGGEGF 356

Query: 368 VRISLIADCDRLGEALDRIKQA 389
            RI+L+       EA++  ++A
Sbjct: 357 FRIALVPTLSECKEAVEVWRRA 378


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: 448
Number of extensions: 22
Number of successful extensions: 6
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: 387
Length adjustment: 31
Effective length of query: 372
Effective length of database: 356
Effective search space:   132432
Effective search space used:   132432
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