GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Echinicola vietnamensis KMM 6221, DSM 17526

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate Echvi_1427 Echvi_1427 amidohydrolase

Query= curated2:A8YUT2
         (384 letters)



>FitnessBrowser__Cola:Echvi_1427
          Length = 397

 Score =  193 bits (491), Expect = 6e-54
 Identities = 122/385 (31%), Positives = 199/385 (51%), Gaps = 15/385 (3%)

Query: 7   SELIQIRRHLHEIPELALQEKETHDYLLKIIKGFNSEFLTIKVPEELPTAILVLIKGSNP 66
           ++ I IRRH+H  PEL+ +E +T  ++ K ++    E     +  +  T ++ LI+G NP
Sbjct: 15  NQTIAIRRHIHAHPELSFEEHQTCAFVEKHLQ----EIGITNIQRKANTGLVALIEGKNP 70

Query: 67  -QRTIGYRTDIDALPVEEKTNLPFSSTHPGIMHACGHDIHMSVALGLLSYFS--ENQPKD 123
            ++ I  R D+DALP+ E+ ++P+ S   G+MHACGHD+H S  LG  S     ++Q + 
Sbjct: 71  SKKVIALRADMDALPIVEQNDVPYKSNKEGVMHACGHDVHTSSLLGAASILHAVKDQFEG 130

Query: 124 NLLFFFQPAEESESGGKKAY-EDGIFEGKFRPDEFYGLHDNPELPAGAIGCREGTLFAGT 182
            +   FQP EE   GG     +D   E   RP    G H  P + AG +G R+G   A  
Sbjct: 131 TVKLIFQPGEEKIPGGASLMIKDKALENP-RPSGIVGQHVMPLIDAGKVGFRKGMYMASA 189

Query: 183 TEVNIDLIGKGGHAAFPQNANDTVVAAASLIMQIQTVISRSIDPIQSGVITLGKVRAGTI 242
            E+ + +IGKGGH A P+   D V+ A+ +I+ +Q VISR+  P    V++ G++ A   
Sbjct: 190 DELYLKVIGKGGHGAMPETLVDPVLIASHIIVALQQVISRNASPKVPSVLSFGRIEALGA 249

Query: 243 RNVIAGQTRIEGTIRGLTQKMILQIDQRLQDLCEGIARSYNMKVNLELNQGGYWPVENNP 302
            NVI  +  I+GT R L +    +  Q++  + EGIA      V+ E+ + GY  ++N P
Sbjct: 250 TNVIPNEVNIQGTFRTLDETWRAEAHQKMVKIAEGIAEGMGGSVDFEVRK-GYPFLQNAP 308

Query: 303 ELT-KNFISYMKNNPEVDFVETKPKMTGEDFGFLLAKFPGTMFWLGVGDPD----SQLHS 357
           ELT + + +      E +  +    M  EDF +   +  G  + LG+ + +    S +H+
Sbjct: 309 ELTDRAYKAAQAYLGEENVEDLDIWMAAEDFSYYTQEMDGCFYRLGIRNEEKGITSGVHT 368

Query: 358 ANLNPDEKSIIRGVNAIKGFLINRM 382
              + DE ++  G   +    IN +
Sbjct: 369 PTFDIDESALEVGAGLMAWIAINEL 393


Lambda     K      H
   0.318    0.138    0.403 

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: 406
Number of extensions: 18
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: 384
Length of database: 397
Length adjustment: 31
Effective length of query: 353
Effective length of database: 366
Effective search space:   129198
Effective search space used:   129198
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 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