GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Beijerinckia indica ATCC 9039

Align Aromatic-amino-acid aminotransferase 2; ARAT-II; AROAT; EC 2.6.1.57 (characterized)
to candidate WP_012386117.1 BIND_RS16265 pyridoxal phosphate-dependent aminotransferase

Query= SwissProt::H3ZPU1
         (389 letters)



>NCBI__GCF_000019845.1:WP_012386117.1
          Length = 410

 Score =  190 bits (482), Expect = 7e-53
 Identities = 120/387 (31%), Positives = 205/387 (52%), Gaps = 20/387 (5%)

Query: 13  SEIRKLFDLAQGIEGIISLGIGEPDFDTPEHIKEYAKEALDKGLTHYSPNIGILELREAV 72
           S I ++F   +G +G+I L +GE D  TP  I E A  +L +G T Y+   G+ ELR A+
Sbjct: 28  SGIVEVFAYGRGRQGLIPLFVGEGDLPTPPFIVEAASRSLTEGETFYTYQAGVPELRAAI 87

Query: 73  AEKFKKHNG------IDADPKTQIMITVGTNQQILMGLATFLKDNEEVLIPSPMFVSYAP 126
           A    +H G      +      Q  +T+G    + + L    + +EEV++P+P + ++  
Sbjct: 88  AAYMSRHYGAIYERTVAPFSPEQFFVTIGGMHALQIALRLVARADEEVIVPTPAWPNFHG 147

Query: 127 AVILAGGKPVEVPTYEENE----FRLSVDELEKYVTPKTRALIINTPNNPTGAVLTKKDL 182
           A+ + G +P+ VP   +N     + L  D +E  +TP TR LI+NTP+NPTG V + KDL
Sbjct: 148 ALSVLGARPITVPMLFQNNGSPGWTLDFDRIEASITPATRCLIVNTPSNPTGWVASLKDL 207

Query: 183 EEIADFAVEHDLMILSDEVYEYFVYDGVKNYSIASLDGMFERTITMNGFSKTFAMTGWRL 242
           E +      H L +++DE+Y    ++G +  S   +    +  + +  FSK +AMTG RL
Sbjct: 208 ETLLALTRRHGLWLVADEIYGRMTFNGERAPSFHDIMEKDDNILFLQTFSKNWAMTGLRL 267

Query: 243 GFLAAPEW---VVEKMVRFQMYNATCPVTFIQYAAAKALRDERSWQAVEEMRREYERRRN 299
           G+L AP     ++E ++++       P    Q AA  AL  E+     ++  R   + R 
Sbjct: 268 GWLEAPRSLAPIIENLIQYSTSGVAVP---WQRAATVAL--EQGEDFFQQSLRRIHQGRT 322

Query: 300 LVWKRLNEMG-LPTVKPKGAFYIFPRIKDTGLSSKEFSELMIKEAKVVVVPGSAFGQAGE 358
           ++++ L + G +   +P+GAFY+F ++      +++ +  +I EA V V PG+AFG  GE
Sbjct: 323 ILYEGLKKTGRIIAAEPEGAFYLFCKVMGE-TDTRQLALRLIDEANVGVAPGTAFGPGGE 381

Query: 359 GYVRISYATAYEKLEEAMDRMEKVLKE 385
            ++R+ +A     L EA+ R+   L++
Sbjct: 382 EFLRLCFARDPALLTEAVRRLSLWLEQ 408


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: 339
Number of extensions: 16
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: 410
Length adjustment: 31
Effective length of query: 358
Effective length of database: 379
Effective search space:   135682
Effective search space used:   135682
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 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