GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Pontibacter ramchanderi LP43

Align Predicted dapE by GapMind curators (no experimental data)
to candidate WP_101443608.1 BD749_RS04195 amidohydrolase

Query= predicted:L0FXC2
         (397 letters)



>NCBI__GCF_002846395.1:WP_101443608.1
          Length = 371

 Score =  255 bits (651), Expect = 2e-72
 Identities = 140/374 (37%), Positives = 213/374 (56%), Gaps = 9/374 (2%)

Query: 21  RRHIHAHPELSFEEHQTCAFVEKHLQEIGITNIQRKANTGLVALIEGKNPSKKVIALRAD 80
           RRHIH HPE+SFEE QT  +VE+ L ++    + + A T L+ +++G  P + V A RAD
Sbjct: 4   RRHIHQHPEVSFEEEQTSKYVEEVLSKLPNVEVIKPAKTSLIGVLKGAKPGRTV-AFRAD 62

Query: 81  MDALPIVEQNDVPYKSNKEGVMHACGHDVHTSSLLGAASILHAVKDQFEGTVKLIFQPGE 140
           MDALPI E+  +PY S ++ V HACGHD HT+ LL  A+ L  ++ + +GTV  IFQ  E
Sbjct: 63  MDALPIQEETGLPYASKEKNVSHACGHDAHTAMLLATAATLSKMQQELKGTVYFIFQHAE 122

Query: 141 EKIPGGASLMIKDKALENPRPSGIVGQHVMPLIDAGKVGFRKGMYMASADELY-LKVIGK 199
           E+ PGGA  +++   L+        G HV+P   AG VG       ++A +++ L +IGK
Sbjct: 123 EQPPGGAIDIVESGELKGVE--AFFGMHVLPNFPAGHVGILPDGAASTAQDIFNLNIIGK 180

Query: 200 GGHGAMPETLVDPVLIASHIIVALQQVISRNASPKVPSVLSFGRIEALGATNVIPNEVNI 259
           G HG+MP   +DP+++ + I+ ALQ V+SRN  P   +V++ G+ ++  A NVI +   +
Sbjct: 181 GSHGSMPHLGIDPIVVGAAIVSALQTVVSRNVEPGEMTVVTIGKFQSGDAFNVIADRAEL 240

Query: 260 QGTFRTLDETWRAEAHQKMVKIAEGIAEGMGGSVDFEVRKGYPFLQNAPELTDRAYKAAQ 319
             + RT  +  R +  Q++ +I E I +  G + + +    YP +QN   L  +  K+A 
Sbjct: 241 AASIRTTSDKTRKQVEQRVKEIIESITKAYGATYELDYINTYPAIQNDKALNAQVRKSAA 300

Query: 320 AYLGEENVEDLDIWMAAEDFSYYTQEMDGCFYRLGIRNEEKGITSGVHTPTFDIDESALE 379
           A LG+E V D  +  A+EDF+YY +     F  LGI     G     H P F +DESAL+
Sbjct: 301 AILGKEQVFDAPMMTASEDFAYYRKIAPVSFMTLGI-----GDGPANHNPGFKVDESALQ 355

Query: 380 VGAGLMAWIAINEL 393
            G      + ++ L
Sbjct: 356 NGVKAQVQLILDYL 369


Lambda     K      H
   0.317    0.134    0.387 

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: 356
Number of extensions: 22
Number of successful extensions: 5
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: 397
Length of database: 371
Length adjustment: 30
Effective length of query: 367
Effective length of database: 341
Effective search space:   125147
Effective search space used:   125147
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 26 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