GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Streptacidiphilus oryzae TH49

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate WP_037575899.1 BS73_RS24325 pyridoxal phosphate-dependent aminotransferase

Query= BRENDA::Q8TQ40
         (389 letters)



>NCBI__GCF_000744815.1:WP_037575899.1
          Length = 398

 Score =  177 bits (449), Expect = 5e-49
 Identities = 117/370 (31%), Positives = 178/370 (48%), Gaps = 7/370 (1%)

Query: 24  AKDEMIAKGVDVIDLGVGDPDLPTHPHIVEAMREAVCDPKTHQYPSYAGMPEFREAAAEW 83
           A+   +A     I+LG G PD      + EA   A+ + + +QYP   G+PE R A AE 
Sbjct: 30  AEMSALATTTGAINLGQGFPDTDGPEAVREAAVRALREGRGNQYPPGPGVPELRAAVAEH 89

Query: 84  CKKYKGIELDPATEVLSLIGSKEAVAHIPLAFVNPGDVVLYTDPGYPVYKIGTLFAGGEP 143
             ++ G++ DP TEVL   G+ EA+A   LA + PGD V+  +P Y  Y      AG + 
Sbjct: 90  QLRFYGLDFDPDTEVLVTAGATEAIAASMLALLEPGDEVIAFEPFYDSYAACIAMAGAKR 149

Query: 144 YSLPLKAENSFLPDLDSIPADILKRAKLFFFNYPNNPTSATADMKFFEKVVEFCKKNDII 203
               L+A  SF PDLD + A I    +L   N P+NPT    D +    +     ++D++
Sbjct: 150 VPFTLRAP-SFRPDLDELRALITPSTRLLLLNSPHNPTGMVLDDEELRAIAALAVEHDLL 208

Query: 204 AVHDNAYSQMVYDGYDAPSFLAAEGAMDIGIELYSHSKTYNMTGWRLGFAVGSKALIKGL 263
            V D  Y  +V++G   P   A  G  +  + + S  KT++ TGW++G+   +  L+  +
Sbjct: 209 VVTDEVYEHLVFEGAHRP-IAALPGMRERTVSISSAGKTFSFTGWKVGWVTAAAPLVAAV 267

Query: 264 GKVKSNVDSGVFDAIQIAGIAALSSSQACVDDTNKIYEERRNVLIEGLTAMGLEVKPPKA 323
              K  +        Q A   AL    A  +D       RR++L  GL A G EV  P+ 
Sbjct: 268 RTAKQYLTYVSAGPFQYAVAEALRLPDAYYEDFRASLRRRRDLLDAGLRAAGFEVYEPQG 327

Query: 324 TFYVWAPV-PTGF-TSIEFAKLLLEEAGIVATPGVGFGD---AGEGYVRFALTKPVERIK 378
           T+++   + P G   +  F + L E  G+VA P   F D   AG   VRF   K  E ++
Sbjct: 328 TYFITTDIAPFGAKDAYAFCRSLPERCGVVAVPNSVFYDDPEAGRSQVRFTFCKKEEVLR 387

Query: 379 EAVERMKKLQ 388
           EA  R+++L+
Sbjct: 388 EAAARLQRLR 397


Lambda     K      H
   0.319    0.137    0.409 

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: 373
Number of extensions: 18
Number of successful extensions: 5
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: 389
Length of database: 398
Length adjustment: 31
Effective length of query: 358
Effective length of database: 367
Effective search space:   131386
Effective search space used:   131386
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 26 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