GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Trichormus variabilis ATCC 29413

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_011319003.1 AVA_RS11210 amidohydrolase

Query= curated2:B7GIC0
         (378 letters)



>NCBI__GCF_000204075.1:WP_011319003.1
          Length = 405

 Score =  253 bits (647), Expect = 5e-72
 Identities = 146/373 (39%), Positives = 205/373 (54%), Gaps = 11/373 (2%)

Query: 3   VNIRRDLHQIPELGFQEFKTQQYILDYLATLPSERLQIKTWRTGILVRVHGTAP-TKTIG 61
           V  RR LHQ PEL FQE  T  ++   L     E  Q    +TGI+  + G  P T+ + 
Sbjct: 28  VEWRRRLHQKPELAFQEKITAAFVSSKLQAWGIEH-QTSIAQTGIVATIKGEKPSTQVLA 86

Query: 62  YRADMDGLPIDEQTDVPFRSTHEGRMHACGHDMHMAIALGVLTHVVHHP--IRDDMLFIF 119
            RADMD LPI E  +VP+ S H G MHACGHD H AIALG   ++  H       +  IF
Sbjct: 87  IRADMDALPIQELNEVPYCSQHNGVMHACGHDGHTAIALGTAYYLQQHRQNFAGTVKIIF 146

Query: 120 QPAEEGPGGALPMLESDEMKQWMPDMILALHIAPAYPVGTIATKEGLLFANTSELFIDLI 179
           QPAEEGPGGA PM+E+  +K    D I+ LH+    P+GT+  + G L A        + 
Sbjct: 147 QPAEEGPGGAKPMIEAGVLKNPDVDAIIGLHLWNNLPLGTVGVRSGPLMAAVELFDCTIF 206

Query: 180 GKGGHAAFPHETKDMVVAASSLIMQLQTIVSRNVNPLDSAVITIGKLTSGTVQNVIAERA 239
           GKGGH A PH+T D VV A+ ++  LQTIV+RNVNP+DSAV+T+G L  GT  NVIA+ A
Sbjct: 207 GKGGHGAIPHQTVDSVVVAAQIVTALQTIVARNVNPIDSAVVTVGALHGGTTHNVIADTA 266

Query: 240 RLEGTIRTLSPEAMEKVKGRIEAIVRGIEVAYDCQAHIDYGSMYYQVYNDETLTNEFMQF 299
            ++GT+R  +P        RIE ++ GI  ++  +    Y  +Y  V ND+ +       
Sbjct: 267 TMKGTVRYFNPAFQGFFPQRIEQVIAGICQSHGAKYDFKYTELYPPVINDQAIAQLVRSV 326

Query: 300 VEK--ETDVHLVRCQEAMTGEDFGYMLARIPGFMFWLGVQSP-----FGLHHAKLNPNEE 352
             +  ET + +V   + M GED  + L  + G  F+LG  +P     +  HH + + +E 
Sbjct: 327 AAEVIETPIGIVPECQTMGGEDMSFFLQEVSGCYFFLGSANPDKDLAYPHHHPRFDFDET 386

Query: 353 AIDVAIQLLTRYV 365
           A+ + +++  R V
Sbjct: 387 ALAMGVEIFVRCV 399


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: 390
Number of extensions: 16
Number of successful extensions: 4
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: 405
Length adjustment: 31
Effective length of query: 347
Effective length of database: 374
Effective search space:   129778
Effective search space used:   129778
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 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