GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Bacillus alkalinitrilicus DSM 22532

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate WP_078429378.1 BK574_RS16655 LL-diaminopimelate aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>NCBI__GCF_002019605.1:WP_078429378.1
          Length = 390

 Score =  166 bits (421), Expect = 8e-46
 Identities = 112/368 (30%), Positives = 179/368 (48%), Gaps = 10/368 (2%)

Query: 21  AKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKT-KYAPPAGIPELREALAE 79
           AK   L ++G D++ L  G PD  TP+H+ ++ + A    K  KY P  G   L+EA+AE
Sbjct: 23  AKVGALVKEGADIINLGQGNPDQPTPDHIVKSLKEAADLPKYHKYPPFRGYRFLKEAVAE 82

Query: 80  KFRRENGLSVTPE-ETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRFAGGV 138
            ++RE G+ + PE E  V  GGK  L  + Q +L+PGD  +V  P +  Y   V  AGG 
Sbjct: 83  FYQREYGVDIDPEKEVCVLFGGKGGLVEISQCMLNPGDVTLVPDPGYPDYWSGVALAGGQ 142

Query: 139 VVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAVEHDF 198
           +  +       F+PD + +      + K + +N PNNPTGA   K   +     A +HD 
Sbjct: 143 MEMMPLQENNNFLPDYQVISEDAKKKAKLMFLNYPNNPTGATASKAFYDETVTFARQHDL 202

Query: 199 YLVSDEIYEHLLYEGE---HFSPGRVAPEHTLTVNGAAKAFAMTGWRIGYACGPKEVIKA 255
            +V D  Y  + ++G+    F     A E  + +   +K + M GWR+ +A G   VI+ 
Sbjct: 203 CVVHDFAYGGIGFDGQKPVSFLQSEGAKEVGIEIYTLSKTYNMAGWRVAFAVGNASVIEM 262

Query: 256 MASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTALGLKAV 315
           +         S     Q A   AL + +     V+   + Y  RR++L+EGL ++G    
Sbjct: 263 LNLYQDHMYVSLFGAIQKAAATALLSPQTC---VDELVKKYEGRRNVLIEGLQSIGWDVK 319

Query: 316 RPSGAFYVLMDTSPIAPDEVRAAERLLEAGVAVVPGTDF--AAFGHVRLSYATSEENLRK 373
            P+G+F+  +        E  A   L +A +AV PG  F  +  G+VR+     E+ L++
Sbjct: 320 APNGSFFAWLPCPEGMSSEEFADILLYKAHIAVAPGRGFGESGEGYVRVGLLEEEDRLKE 379

Query: 374 ALERFARV 381
           A+ER  ++
Sbjct: 380 AVERIRKL 387


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: 378
Number of extensions: 17
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: 385
Length of database: 390
Length adjustment: 30
Effective length of query: 355
Effective length of database: 360
Effective search space:   127800
Effective search space used:   127800
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