GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Sinorhizobium medicae WSM419

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (characterized)
to candidate WP_011974383.1 SMED_RS00865 M20 aminoacylase family protein

Query= SwissProt::D5E0A1
         (375 letters)



>NCBI__GCF_000017145.1:WP_011974383.1
          Length = 388

 Score =  229 bits (583), Expect = 1e-64
 Identities = 138/372 (37%), Positives = 191/372 (51%), Gaps = 7/372 (1%)

Query: 5   EFVKIRRELHKIPELGFQEVKTQRFLLDYINTLPQERLEVKTWKTGLFVKVHGTNPTKTI 64
           E V IRR+ H  PELG  E +T  F+  ++  L  E +     KTG+   +     +++I
Sbjct: 13  ELVAIRRDFHAHPELGLAETRTSAFVARHLEALGFE-VTTGLAKTGVVGTLSCGTGSRSI 71

Query: 65  GYRADIDGLPITEETNYSFQSQHEGLMHACGHDMHMAIGLGVLTYFAQHE-IKDNVLFIF 123
           G RAD+D LPI EET   + S+  GLMHACGHD H A+ LG     A+ +     +  IF
Sbjct: 72  GIRADMDALPIAEETGLDYASKTPGLMHACGHDGHTAMLLGAARALAERKNFNGTIHLIF 131

Query: 124 QPAEEGPGGAQPMLQSDIMKEWLPDFIFALHVAPEYPVGSIALKEGLLFANTSELFIDLK 183
           QPAEE  GGA+ M+   + + +  D +FALH  P  P G  AL +G + A   E  I + 
Sbjct: 132 QPAEENAGGAKIMVDEGLFERFPCDAVFALHNEPNLPFGQFALCDGPIMAAVDEARITVH 191

Query: 184 GKGGHAAYPHTTNDMVVAACQLVSQLQTIVARNVDPLDSAVITVGKIQGGTVQNIIAERA 243
           G+GGH A P  T D +V    +V  LQT+VARN+ P+D +V+TVG    G+  NII ERA
Sbjct: 192 GRGGHGAEPQETADPIVCGASIVMALQTVVARNIHPMDPSVVTVGAFHAGSASNIIPERA 251

Query: 244 RIEGTIRTLSPESMTRVKERIEAIVKGVEVGYQCETAIDYGCMYHQVYNHHEVTREFMEF 303
            I   IR+  P     ++ RI  I K     +     +DY   Y    NH   T    E 
Sbjct: 252 EIVVGIRSFDPAVRDELERRIRMIAKSQAESFGMRATVDYERSYDATVNHKAETDFLRET 311

Query: 304 AKEQTDVD-VIECKEAMTG-EDFGYMLKDIPGFMFWLGVQ---SEYGLHHAKLQPHEGAI 358
           A      D V++ +    G EDF YMLK+ PG  F+LG +    E  LHH     ++  +
Sbjct: 312 AIRFAGADHVVDLQRPFMGSEDFAYMLKERPGSYFFLGSRVTGEEKSLHHPGYNFNDDLL 371

Query: 359 DIAISLITKYFE 370
            I ++  T+  E
Sbjct: 372 PIGVAFWTELAE 383


Lambda     K      H
   0.320    0.137    0.410 

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: 363
Number of extensions: 20
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: 375
Length of database: 388
Length adjustment: 30
Effective length of query: 345
Effective length of database: 358
Effective search space:   123510
Effective search space used:   123510
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 Jul 25 2024. The underlying query database was built on Jul 25 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