GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Caulobacter crescentus NA1000

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate CCNA_02900 CCNA_02900 N-acyl-L-amino acid amidohydrolase

Query= curated2:Q032G8
         (376 letters)



>FitnessBrowser__Caulo:CCNA_02900
          Length = 437

 Score =  155 bits (392), Expect = 2e-42
 Identities = 119/367 (32%), Positives = 185/367 (50%), Gaps = 30/367 (8%)

Query: 9   RQLHQIPEIGLEEHKTQKYLLTIIHQIIQNKSFIQVE-TWQTGILVYLKGSQGQKTIGWR 67
           + +H  PE+G +E +T K L   +  +     F   E   +TG++  LK  +G K +  R
Sbjct: 48  KDIHAHPELGFQEVETAKKLAAQMRAL----GFTVTEGVGKTGVVAVLKNGEGPKVL-IR 102

Query: 68  TDIDGLPVEELTNLPFASK-----NGRM----HACGHDIHMTVALGLLEKL--SESQPKN 116
           T++DGLP++E + L +AS+     NG      HACGHDIHM   +G   +L   +++ K 
Sbjct: 103 TELDGLPMQEKSGLAWASQATATWNGEKVFVAHACGHDIHMAAWVGAARQLVAMKAKWKG 162

Query: 117 NLLFLFQPAEENEAGGKLMYDGGAFKN--WLPDEFYGLHVRPDLKVGDIATNEQTLFAGT 174
            L+F+ QP+EE   G + M D G +      PD  + LHV      G++      L + +
Sbjct: 163 TLVFVAQPSEETVRGARAMLDDGLWDKIGGKPDYGFALHVGSG-PAGEVYYKAGVLTSTS 221

Query: 175 CEVELTFVGTGGHAAFPHTANDALVAAAYFVTQVQTIVSRNVDPLDSAVVTFGKMEAGTT 234
             +++TF G GGH + P    D ++ AA F   VQ+++SR  DP    VVT G ++AG+ 
Sbjct: 222 DGLDITFNGRGGHGSMPSATIDPVLMAARFTVDVQSVISREKDPSAFGVVTVGSIQAGSA 281

Query: 235 NNIIAERAFLHGTIRSLTQEVNELTQKRLTELAKGVAQSFDMT----IDLKLKQGGYLPV 290
            NII ++A + GTIR  TQ+ N + +K L  + + V    DM      DLKL  GG + V
Sbjct: 282 GNIIPDKARVRGTIR--TQD-NAVREKILDGVRRTVKAVTDMAGAPPADLKLTPGGKM-V 337

Query: 291 ENNPKLAKELMDFFRNETKANLI-DIAPAMTGEDFG-YLLSKIPGVMFWLGINSEAPLHS 348
            N+  L       F+    A  +    P    ED+  ++L+ +P V F +G +  A L  
Sbjct: 338 VNDAALTDRTAVVFKAAFGARAVAQDKPGSASEDYSEFVLAGVPSVYFAIGGSDPAELAK 397

Query: 349 QKMQADE 355
            K +  E
Sbjct: 398 AKAEGRE 404


Lambda     K      H
   0.319    0.136    0.396 

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: 326
Number of extensions: 13
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: 376
Length of database: 437
Length adjustment: 31
Effective length of query: 345
Effective length of database: 406
Effective search space:   140070
Effective search space used:   140070
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 (21.7 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