GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Beijerinckia indica subsp. indica ATCC 9039

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate WP_012386117.1 BIND_RS16265 pyridoxal phosphate-dependent aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>NCBI__GCF_000019845.1:WP_012386117.1
          Length = 410

 Score =  162 bits (411), Expect = 1e-44
 Identities = 120/369 (32%), Positives = 177/369 (47%), Gaps = 22/369 (5%)

Query: 28  RQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPELREALAEKFRRENGL 87
           RQG  L+ L  GE D  TP  + EAA R+L +G+T Y   AG+PELR A+A    R  G 
Sbjct: 40  RQG--LIPLFVGEGDLPTPPFIVEAASRSLTEGETFYTYQAGVPELRAAIAAYMSRHYGA 97

Query: 88  -------SVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRFAGGVVV 140
                    +PE+  VT+GG  AL    + +    +EVIV +P W ++   +   G   +
Sbjct: 98  IYERTVAPFSPEQFFVTIGGMHALQIALRLVARADEEVIVPTPAWPNFHGALSVLGARPI 157

Query: 141 EVETLPEE----GFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAVEH 196
            V  L +     G+  D +R+  +ITP T+ L+VN+P+NPTG V   + LE L  L   H
Sbjct: 158 TVPMLFQNNGSPGWTLDFDRIEASITPATRCLIVNTPSNPTGWVASLKDLETLLALTRRH 217

Query: 197 DFYLVSDEIYEHLLYEGEH---FSPGRVAPEHTLTVNGAAKAFAMTGWRIGYACGPKEVI 253
             +LV+DEIY  + + GE    F       ++ L +   +K +AMTG R+G+   P+ + 
Sbjct: 218 GLWLVADEIYGRMTFNGERAPSFHDIMEKDDNILFLQTFSKNWAMTGLRLGWLEAPRSLA 277

Query: 254 KAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTALG-L 312
             + ++   ST+      Q A   AL   E    F + +     + R +L EGL   G +
Sbjct: 278 PIIENLIQYSTSGVAVPWQRAATVAL---EQGEDFFQQSLRRIHQGRTILYEGLKKTGRI 334

Query: 313 KAVRPSGAFYVLMDTSPIAPDEVRAAERLLEAGVAVVPGTDFAAFGH--VRLSYATSEEN 370
            A  P GAFY+             A   + EA V V PGT F   G   +RL +A     
Sbjct: 335 IAAEPEGAFYLFCKVMGETDTRQLALRLIDEANVGVAPGTAFGPGGEEFLRLCFARDPAL 394

Query: 371 LRKALERFA 379
           L +A+ R +
Sbjct: 395 LTEAVRRLS 403


Lambda     K      H
   0.317    0.133    0.379 

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: 404
Number of extensions: 19
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: 385
Length of database: 410
Length adjustment: 31
Effective length of query: 354
Effective length of database: 379
Effective search space:   134166
Effective search space used:   134166
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