GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Sinorhizobium meliloti 1021

Align 1-piperideine-2-carboxylate/1-pyrroline-2-carboxylate reductase (NADPH) (EC 1.5.1.21) (characterized)
to candidate SM_b20261 SM_b20261 malate dehydrogenase

Query= BRENDA::Q9I492
         (334 letters)



>FitnessBrowser__Smeli:SM_b20261
          Length = 345

 Score =  356 bits (914), Expect = e-103
 Identities = 183/331 (55%), Positives = 224/331 (67%), Gaps = 1/331 (0%)

Query: 4   MTLDEVRELAVRILRRHAFSEAHVQAVADTLVAGERDECASHGIWRLLGCIATLKAGKVS 63
           +T   ++E    I R+   +     A+A  +VAGERD C SHGI+R+ G + T+KAGKV 
Sbjct: 7   LTTTALQERVEAIFRKGGLNVVQAGALARVIVAGERDACKSHGIYRIEGALRTVKAGKVK 66

Query: 64  ADAEPEL-HDIAPGLLRVDAHGGFSQCAFRLGLPHLLEKARSQGIAAMAVNRCVHFSALW 122
            DAEPE+    A  +++V+A GGF+  AF LGLP L E+AR  GIAA+A+N C HFSALW
Sbjct: 67  PDAEPEIVAQEASAIVKVNAGGGFANPAFELGLPVLAERARKHGIAALAINDCTHFSALW 126

Query: 123 VEVEALTEAGLVALATTPSHAWVAPAGGRKPIFGTNPIAFGWPRPDGPPFVFDFATSAVA 182
            E EALT  GL  L   PS+A VAP GG KP+ GTNP AFGWPR   PP+VFDFATS  A
Sbjct: 127 PEAEALTGEGLAGLVMCPSYATVAPTGGNKPLLGTNPFAFGWPRAGKPPYVFDFATSVAA 186

Query: 183 RGEIQLHERAGKPIPLGWGVDEQGEPTTDASAALRGAMLTFGGHKGSALAAMVELLAGPL 242
           RGEI+LH RAGKP+P GW +D QG PTTD  AAL GAML FGGHKGSA+  M+ELLAG +
Sbjct: 187 RGEIELHRRAGKPLPEGWAIDAQGNPTTDPEAALAGAMLPFGGHKGSAIGTMIELLAGIM 246

Query: 243 IGDLTSAESLAYDEGSRSSPYGGELLIAIDPRRMLGASAEEHLARAETLFEGIVEQGARL 302
           IGDLTS E L Y   +  +P+ GEL++A  P+        +  ARAE LFE IV QGARL
Sbjct: 247 IGDLTSPEVLDYLGTTTLAPFHGELIVAFSPQAFAAGRPGDPFARAELLFEAIVGQGARL 306

Query: 303 PSQRRFEARERSARDGVTIPEALHRELLALL 333
           PSQRRF AR +S  +G+T+  A   +L  LL
Sbjct: 307 PSQRRFAARAKSEAEGITLSAAEIEQLDRLL 337


Lambda     K      H
   0.320    0.136    0.407 

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: 386
Number of extensions: 19
Number of successful extensions: 2
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: 334
Length of database: 345
Length adjustment: 28
Effective length of query: 306
Effective length of database: 317
Effective search space:    97002
Effective search space used:    97002
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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