GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Acidovorax sp. GW101-3H11

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate Ac3H11_1969 N-acetyl-L,L-diaminopimelate deacetylase (EC 3.5.1.47)

Query= curated2:B7GIC0
         (378 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1969
          Length = 447

 Score =  188 bits (477), Expect = 3e-52
 Identities = 127/376 (33%), Positives = 187/376 (49%), Gaps = 28/376 (7%)

Query: 3   VNIRRDLHQIPELGFQEFKTQQYILDYLATLPSERLQIKTWRTGILVRVHGTAPTKTIGY 62
           VN RRD+H  PEL  QE +T + + ++L  L  E +Q     TG++  + G  P K +  
Sbjct: 50  VNWRRDIHAYPELSGQEVRTAKLVAEHLKKLGME-VQTGVGGTGVVGTLKGGLPGKVVAL 108

Query: 63  RADMDGLPIDEQTDVPFRS----THEGR----MHACGHDMHMAIALGVLTHV--VHHPIR 112
           RADMD LP+ E T +PF S    T+ G+    MHACGHD H A+ +G    +  +   + 
Sbjct: 109 RADMDALPVLENTGLPFASKAKATYLGKEVPVMHACGHDAHTAMLMGAAEVLAGMKAQLP 168

Query: 113 DDMLFIFQPAEEGPG------------GALPMLESDEMKQWMPDMILALHIAPAYPVGTI 160
             + FIFQPAEEG              GA  M+E+  +K      I  LHI    P G +
Sbjct: 169 GTVKFIFQPAEEGAPVEADANGKVPSFGAKAMIEAGALKD--VQAIYGLHITSNLPGGVV 226

Query: 161 ATKEGLLFANTSELFIDLIGKGGHAAFPHETKDMVVAASSLIMQLQTIVSRNVN-PLDSA 219
             + G L A +  + I + G+GGH + P  T D +VAAS ++M LQT+VSR +N   + A
Sbjct: 227 GYRSGPLMAGSDNITIHVEGRGGHGSSPWATIDPIVAASQVVMGLQTVVSRQLNISQEPA 286

Query: 220 VITIGKLTSGTVQNVIAERARLEGTIRTLSPEAMEKVKGRIEAIVRGIEVAYDCQAHIDY 279
           V+TIG++  GT  N+I ++  + GT+RT   +  ++   RI      I  A   +A + +
Sbjct: 287 VVTIGQIQGGTRYNIIPDKVEMMGTLRTFDEDMRQEALKRITTTAESIAAASGAKASVRF 346

Query: 280 GSMYYQV-YNDETLTNEFMQFVEKETDVHLVRCQEAMTGEDFGYMLARIPGFMFWLGVQS 338
           G + Y V  N   LT   +  +        +   +    EDF      +PGF ++LG   
Sbjct: 347 GPVAYPVTTNPAQLTQASLPALNLAMGGKTMVIPKVAGSEDFSEFQKVVPGFFYFLGA-P 405

Query: 339 PFGLHHAKLNPNEEAI 354
           P G   AK  PN  A+
Sbjct: 406 PKGKEFAKAPPNHSAL 421


Lambda     K      H
   0.322    0.137    0.411 

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: 372
Number of extensions: 17
Number of successful extensions: 7
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: 378
Length of database: 447
Length adjustment: 31
Effective length of query: 347
Effective length of database: 416
Effective search space:   144352
Effective search space used:   144352
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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