GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Sinorhizobium meliloti 1021

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate SMc02087 SMc02087 type II citrate synthase

Query= reanno::pseudo6_N2E2:Pf6N2E2_6062
         (375 letters)



>FitnessBrowser__Smeli:SMc02087
          Length = 429

 Score =  181 bits (458), Expect = 4e-50
 Identities = 123/372 (33%), Positives = 183/372 (49%), Gaps = 37/372 (9%)

Query: 32  LTYRGYDVRDLAADAQFEEVAYLLLYGELPTQAQLDAYTGKLRQLRDLPQALKEVLERIP 91
           L +RG+ +  LA    F EV YLLLYGELPT+AQ   +  ++     + + +        
Sbjct: 67  LLHRGFPIEQLAEHGDFLEVCYLLLYGELPTKAQKADFDYRVTHHTMVHEQMSRFFTGFR 126

Query: 92  ADAHPMDVMRTGCSFLGNLEPEQDFSQQHDKTD------------RLLAAFPAIMCYWYR 139
            DAHPM VM   C  +G L      +  HD TD            R++A  P I    Y+
Sbjct: 127 RDAHPMAVM---CGCVGALS-----AFYHDSTDITDPHQRMVASLRMIAKMPTIAAMAYK 178

Query: 140 FSHQGQRIECVTDEVSIGGHFLHLLHGKKPSELHV-----KVMNVSLILYAEHEFNASTF 194
           + H GQ      +++    +FL +       E  V     + M+   IL+A+HE NAST 
Sbjct: 179 Y-HIGQPFVYPKNDLDYASNFLRMCFAVPCEEYVVNPVLARAMDRIFILHADHEQNASTS 237

Query: 195 TARVCASTLSDLFSCITAAIGSLRGPLHGGANEAAMEMIERFSSPQEAIEGTLGMLARKD 254
           T R+  S+ ++ F+CI A I  L GP HGGANEAA+ M+    +     E       + D
Sbjct: 238 TVRLAGSSGANPFACIAAGIACLWGPAHGGANEAALNMLAEIGTVDRIPEYITKAKDKND 297

Query: 255 --KIMGFGHAIYKDNDPRNEVIKGWSKKLADEVG--DTVLFPVSEAIDK-----TMWEQK 305
             ++MGFGH +YK+ DPR ++++  + ++  E+G  D  L  V+  +++       + +K
Sbjct: 298 PFRLMGFGHRVYKNYDPRAKIMQKTTHEVLAELGHKDDPLLEVAMELERIALTDEYFIEK 357

Query: 306 KLFPNADFYHASAYHFMGIPTKLFTPIFVCSRLTGWAAHVFE--QRANNRIIRPSAEYTG 363
           KL+PN DFY       +G PT +FT +F  +R  GW A   E  +    RI RP   Y G
Sbjct: 358 KLYPNIDFYSGITLKALGFPTTMFTVLFALARTVGWIAQWNEMIEDPEQRIGRPRQLYVG 417

Query: 364 VEQRKFVPIEQR 375
              R +VPI +R
Sbjct: 418 APLRDYVPISKR 429


Lambda     K      H
   0.321    0.135    0.406 

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: 425
Number of extensions: 36
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: 375
Length of database: 429
Length adjustment: 31
Effective length of query: 344
Effective length of database: 398
Effective search space:   136912
Effective search space used:   136912
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 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