GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Methanosarcina acetivorans C2A

Align Aromatic-amino-acid aminotransferase 2; ARAT-II; AROAT; EC 2.6.1.57 (characterized)
to candidate WP_048064998.1 MA_RS04795 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= SwissProt::H3ZPU1
         (389 letters)



>NCBI__GCF_000007345.1:WP_048064998.1
          Length = 393

 Score =  343 bits (881), Expect = 4e-99
 Identities = 166/385 (43%), Positives = 257/385 (66%), Gaps = 3/385 (0%)

Query: 3   LSDRLEMVNPSEIRKLFDLAQGIEGIISLGIGEPDFDTPEHIKEYAKEALDKGLTHYSPN 62
           +++ ++ + PS IR+ FDL  G+E IISLG+GEPDF TP HI+E    +L+KG T Y+ N
Sbjct: 11  VAEAVKSIPPSGIRRFFDLVSGLEDIISLGVGEPDFITPWHIREMCIHSLEKGQTSYTSN 70

Query: 63  IGILELREAVAEKFKKHNGIDADPKTQIMITVGTNQQILMGLATFLKDNEEVLIPSPMFV 122
            G+ ELR+ +A  + K  G+D DP ++I++T G ++ + + +   +   EEV++  P +V
Sbjct: 71  YGLPELRDELARTYYKRYGLDYDPASEILVTTGVSEALDIAVRAVVNPGEEVIVVQPSYV 130

Query: 123 SYAPAVILAGGKPVEVPTYEENEFRLSVDELEKYVTPKTRALIINTPNNPTGAVLTKKDL 182
           +Y P+VILAGGKPV V T  +++F L+ + L+  +T KT+A+I+N PNNPTGA++ ++ +
Sbjct: 131 AYVPSVILAGGKPVIVSTSRDDDFSLTAEALKPAITSKTKAIILNFPNNPTGAIMEQEGM 190

Query: 183 EEIADFAVEHDLMILSDEVYEYFVYDGVKNYSIASLDGMFERTITMNGFSKTFAMTGWRL 242
           E+IAD  VE+DL ++SDEVYE   Y G  +   +SL+G+ +RT+ +NGFSK +AMTG RL
Sbjct: 191 EDIADLVVENDLFVISDEVYECLTYGGT-HVPFSSLEGLKDRTVMLNGFSKAYAMTGLRL 249

Query: 243 GFLAAPEWVVEKMVRFQMYNATCPVTFIQYAAAKALRDERSWQAVEEMRREYERRRNLVW 302
           GF      ++  M+    Y+  C     Q  A +ALR+ +  + +E M REY+RRR  + 
Sbjct: 250 GFAMGAPDIIHSMMMIHQYSMLCAPITAQVGAIEALRNGK--EEMERMVREYDRRRRFIV 307

Query: 303 KRLNEMGLPTVKPKGAFYIFPRIKDTGLSSKEFSELMIKEAKVVVVPGSAFGQAGEGYVR 362
           K  N +GL    PKGAFY FP I  TGLSS +F+E +++E KVV +PG  FG+AGEG++R
Sbjct: 308 KGFNSIGLECGNPKGAFYAFPYIGGTGLSSSDFAERLLEEKKVVTIPGDVFGEAGEGFLR 367

Query: 363 ISYATAYEKLEEAMDRMEKVLKEKK 387
            +YA + + + ++++RM   ++E K
Sbjct: 368 CAYAASLDDIRKSIERMGDFVEELK 392


Lambda     K      H
   0.318    0.135    0.387 

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: 375
Number of extensions: 22
Number of successful extensions: 3
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: 393
Length adjustment: 31
Effective length of query: 358
Effective length of database: 362
Effective search space:   129596
Effective search space used:   129596
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: 50 (23.9 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