GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Thermus aquaticus YT-1

Align Probable aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.78; Transaminase A (uncharacterized)
to candidate WP_053767116.1 BVI061214_RS02250 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= curated2:O33822
         (383 letters)



>NCBI__GCF_001280255.1:WP_053767116.1
          Length = 356

 Score =  127 bits (319), Expect = 5e-34
 Identities = 115/356 (32%), Positives = 169/356 (47%), Gaps = 23/356 (6%)

Query: 32  DLVALTAGEPDFDTPEHVKEAGRRALAQGKTKYAPPAGIPELREAVAEKFRRENGLEVTP 91
           D++ L   + DF   E ++ A  +A A+G   Y P  G  EL+  + E+   +  +   P
Sbjct: 18  DVLPLWVADMDFPVAEPIRRA-IQARAEGFLGYPPREGDKELKALLLERTGLQGEVAFMP 76

Query: 92  EETIVTVGGKQALFNLFQAILDPGDEVIVLAPYWVSYPEMVRFAGGVPVEVPTLPEE-GF 150
               V VG    L+    A   PG  V+   P +  +   +R  G   +  P    E G+
Sbjct: 77  G---VVVG----LYAAVAAFTAPGHGVLTQVPVYPPFLSAIREQGRTLLANPLKETEAGY 129

Query: 151 VPDPERVRRAITPRTKALVVNSPNNPTGVVYPEEVLRALAEMALQHDFYLVSDEIYEHLI 210
             D   + R +   ++ L+   P NPTG V+ EE L ALA++A +HD  +VSDE++  L 
Sbjct: 130 RLDLGGLER-LAYASRLLLFCHPQNPTGRVFTEEELSALAQVARKHDLVVVSDELHAPLT 188

Query: 211 YEGAHFSPGTLAPEHTITVNGAAKAFAMTGWRIGYACGPKAVIKAMADVSSQSTTSPDTI 270
           YE  H       PE TIT+ G  KA+ + G  +G A GPK +++A+        T P+ +
Sbjct: 189 YERPHIPLARFLPERTITLLGPGKAYNLAGLPMGAAVGPKPLVEALK--RHLPHTFPNVL 246

Query: 271 AQWATLEALTNREASMAFIAMAREAYRKRRDLLLEGLSRIGLEAVRPSGAFYVLMDTSPF 330
           A  A   AL   E    ++       R+ RD L      +GL  V P G  Y+     PF
Sbjct: 247 AMAAWKAALLEGE---GWLREVLGMLRQNRDRLAAWAQEMGLFHVPPEGT-YLAWLRMPF 302

Query: 331 APNEVEAAERLL-MAGVAVVPGTEFAA--FGHVRLSYATGEENLKKALERFAQALQ 383
                +AA RLL  A VA+ PG  F      +VRL++AT  E L++AL R AQAL+
Sbjct: 303 P----KAASRLLEEARVALNPGENFGKGYDRYVRLNFATYPEVLEEALSRMAQALK 354


Lambda     K      H
   0.317    0.133    0.382 

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: 371
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: 383
Length of database: 356
Length adjustment: 30
Effective length of query: 353
Effective length of database: 326
Effective search space:   115078
Effective search space used:   115078
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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