GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Clostridium acetobutylicum ATCC 824

Align Aspartate aminotransferase; AspAT; EC 2.6.1.1; Transaminase A (uncharacterized)
to candidate NP_348995.1 CA_C2380 PLP-dependent aminotransferase

Query= curated2:O58489
         (391 letters)



>NCBI__GCF_000008765.1:NP_348995.1
          Length = 395

 Score =  281 bits (719), Expect = 2e-80
 Identities = 158/376 (42%), Positives = 238/376 (63%), Gaps = 9/376 (2%)

Query: 16  IKRSKIRELFERASKMEDVISLGIGEPDFDTPKNIKEAAKRALDEGWTHYTPNAGIPELR 75
           I+ S IR+ + +  K++  ISL +G+PDF  P  +K A  RA+++  T YT NAGI ELR
Sbjct: 21  IQISGIRKFYNKVIKVQGAISLTLGQPDFPVPDKVKRAMVRAIEDNKTVYTSNAGIDELR 80

Query: 76  EAVVEYYKKFYGIDIEVENVIITAGAYEGTYLAFESLLERGDEVIIPDPAFVSYAEDAKV 135
             + +Y K+F  I+   + + ITAG  EG    F++LL +GD+V++PDP+F +YA   K+
Sbjct: 81  NEISKYLKRF-NINYSKDEICITAGGTEGILDIFQALLNKGDKVLVPDPSFPAYASCTKL 139

Query: 136 AEAKPVRIPLREENNFLPDPNELLEKI-SKNTRMIVINYPNNPTGATLDKELAKTIADIA 194
            E + +   L   + F  D NEL  KI ++  + +V++YP+NPTG  + KE  + +  I 
Sbjct: 140 LEGEVITYGLYG-SEFSIDFNELENKIKNEKPKFMVLSYPSNPTGTVISKEDNEKLHKII 198

Query: 195 EDYNIYILSDEPYEHFIYEDAKHYPMIKFAP--ENTILANSFSKTFAMTGWRLGFVVAPS 252
           +D +I  ++DE Y    YED  +Y + ++    E  I+ + FSKTF+MTG R+G+V A S
Sbjct: 199 KDNDIIAVTDEMYSALCYED-DYYSVSQYEDIREKVIVVSGFSKTFSMTGLRIGYVCAES 257

Query: 253 QVIKEMTKLHAYVIGNVASFVQIAGIEALRSEESWKAVEEMKKEYNERRKIVVKRLKNMP 312
             +  + K+H Y      S  Q   +E L++ +  + V+ MK E+ +RR  V KRLK+M 
Sbjct: 258 SFMSSILKVHQYTTTCAPSISQYGALEGLKNCD--EDVQYMKNEFKKRRDYVYKRLKDM- 314

Query: 313 GIKVKEPKGAFYVFPNISGTGMSSEKFSEWLLEKARVVVIPGTAFGRMGEGYVRISYATS 372
           G +V+ PKGAFY+FP+IS  GM+SE+F E LL +A+V ++PG+AFG  GEG+ RISYA S
Sbjct: 315 GFEVRLPKGAFYIFPDISRFGMTSEQFCEKLLNEAKVAIVPGSAFGEKGEGFARISYAYS 374

Query: 373 KEKLIEAMNRIEKALE 388
           K++L E MNRIEK +E
Sbjct: 375 KKELEECMNRIEKWVE 390


Lambda     K      H
   0.316    0.135    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: 429
Number of extensions: 27
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: 391
Length of database: 395
Length adjustment: 31
Effective length of query: 360
Effective length of database: 364
Effective search space:   131040
Effective search space used:   131040
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 (21.6 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