GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Methanobacterium lacus AL-21

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_013646093.1 METBO_RS12525 amidohydrolase

Query= curated2:Q88V24
         (384 letters)



>NCBI__GCF_000191585.1:WP_013646093.1
          Length = 417

 Score =  157 bits (396), Expect = 7e-43
 Identities = 118/381 (30%), Positives = 183/381 (48%), Gaps = 28/381 (7%)

Query: 12  YQHLHQIPEIGLQEHETQAYLLSIIGKMPQEWLTIKTIPTLDTAILVKVSGLKHDYRIGY 71
           +Q LHQ PE+  QE E+  Y+ S +  +  + L +   P   T I   + G      +  
Sbjct: 25  FQWLHQHPELAYQEFESGRYIASYLETL--DGLEV-IYPFAKTGIKAVLKGENSKNAVAI 81

Query: 72  RTDIDALPVTENTGLPFASTHPG--------VMHACGHDIHMSVALGILSYFAENRPAT- 122
           R D DALPV E+TGL +AS   G        V H CGHD   + A+G  +   + +    
Sbjct: 82  RADFDALPVKEDTGLSYASRSKGTYNGQETYVSHVCGHDASAATAMGTATVLNQLKDDLN 141

Query: 123 -DMVFMFQPAEENASGGQR-----LYESGALDGDWMPD--EIFAFHDNPNLPTGAIGCRM 174
            D+VF+FQPAEE    G +     +   GAL     PD   IFA H       G +    
Sbjct: 142 GDVVFLFQPAEEGVPDGMKAGADLMVSEGALKN---PDVSAIFALHPYSKAYPGTVLLSK 198

Query: 175 GTLFAGTCEIHAHLSGKSGHAAYPHQANDMVVAGAALVSQLQTIVARNVDPIQ-SGVVTL 233
            T  AG  ++   + G   H + P    D +VAGAA+++ LQTIV+R  D ++ + VVT+
Sbjct: 199 NTTHAGLNDLVIKIKGVQAHGSMPWVGRDPIVAGAAIINSLQTIVSREADLMRGAAVVTV 258

Query: 234 GHFTAGTIGNVIAGEAQIDGTIRALTQEMNMHIQRRVRTITEGIALAYDCNIDLKLNQGG 293
           G+F  G   N+I   A++  TIRAL +     + +RV  IT+ ++ A+ C  ++ + Q  
Sbjct: 259 GYFHGGIKVNIIPDHAEMGLTIRALDENNLKLLVKRVTEITKLVSKAHGCEAEIIMGQ-- 316

Query: 294 YYPVENNDA-ITADFIKYMQEDDDVNFIETEPAMTG-EDFGYLIHQIPGTMFWLGVDSPY 351
           + P+  ND  +  + +K +++      +  +PA TG EDF Y  +++PG     G     
Sbjct: 317 HDPMNKNDPDLCKNMLKTIRQVAGDGNMILKPATTGSEDFSYFSNKVPGLYLHFGTAPQN 376

Query: 352 SLHSENMVPHTAAIMSGVNAM 372
              SE+   H    M   +A+
Sbjct: 377 KPLSESRPNHHPGFMVDDDAL 397


Lambda     K      H
   0.320    0.136    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: 441
Number of extensions: 26
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: 384
Length of database: 417
Length adjustment: 31
Effective length of query: 353
Effective length of database: 386
Effective search space:   136258
Effective search space used:   136258
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 (21.8 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