GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Phaeobacter inhibens BS107

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate GFF998 PGA1_c10150 amidohydrolase

Query= curated2:B1YJ90
         (370 letters)



>FitnessBrowser__Phaeo:GFF998
          Length = 388

 Score =  237 bits (605), Expect = 4e-67
 Identities = 141/355 (39%), Positives = 199/355 (56%), Gaps = 7/355 (1%)

Query: 8   RRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGL--TGNRTIGYR 65
           RR LH+IPE  ++  KT AF+ +++RS+    ++     TGV   ++G   T  R IG R
Sbjct: 18  RRHLHQIPELLYEVHKTAAFVEEKLRSFGITDITTGIGRTGVVAVIEGKANTSGRVIGLR 77

Query: 66  ADIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVELPVMDD-VVFLFQPA 124
           AD+D LPI EATGL + S+ PG MHACGHD H SI LG  + + E    D  VV +FQPA
Sbjct: 78  ADMDALPITEATGLDYASQTPGLMHACGHDGHTSILLGTAKYLAETRNFDGKVVLIFQPA 137

Query: 125 EEGPGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVHITIYGQS 184
           EEG  G + M    + +++   E+YGLH AP  PVG  A RPG L AS+ E  I + G  
Sbjct: 138 EEGGAGGKAMCDDGMMDRWGIQEVYGLHNAPGIPVGEFAIRPGPLLASSDEFEIIVTGVG 197

Query: 185 GHAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDA-GIRENVIAGRALL 243
           GHAA PH  IDT +  + +++ L +IVSR+I+P+   V+T+G  +      NVIA  A L
Sbjct: 198 GHAANPHEAIDTTLVASQIVVSLHSIVSRNIDPLKHVVLTVGTFETDSTASNVIAHTARL 257

Query: 244 DGTMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVNDQRVVDKFSSFVK 303
            GT+R L      + E RVR I   + +++G + ++ +   Y   VN +          +
Sbjct: 258 QGTVRTLETECRGQAEIRVRRIAEDVASAYGARAEVVWTPGYPVTVNTETETGYAVEAAR 317

Query: 304 MNANYI--ECDAAMTGEDFGFMLKEIPGMMFWLGVNNATSGLHQPTLNPDEEAIP 356
             A  +  + D  M  EDF +ML+E PG   +LG N  T+  H P  + D+EAIP
Sbjct: 318 AVAAKVTDDTDPIMPSEDFAYMLEERPGAYIFLG-NGDTAMCHHPAYDFDDEAIP 371


Lambda     K      H
   0.323    0.140    0.417 

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: 410
Number of extensions: 16
Number of successful extensions: 6
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: 370
Length of database: 388
Length adjustment: 30
Effective length of query: 340
Effective length of database: 358
Effective search space:   121720
Effective search space used:   121720
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 09 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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