GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Synechococcus elongatus PCC 7942

Align citrate synthase (unknown stereospecificity) (EC 2.3.3.16) (characterized)
to candidate Synpcc7942_0612 Synpcc7942_0612 methylcitrate synthase

Query= BRENDA::P45858
         (372 letters)



>FitnessBrowser__SynE:Synpcc7942_0612
          Length = 386

 Score =  243 bits (619), Expect = 8e-69
 Identities = 143/370 (38%), Positives = 207/370 (55%), Gaps = 8/370 (2%)

Query: 1   MEEKQHYSPGLDGVIAAETHISYLDTQSSQILIRGYDLIELSETKSYLELVHLLLEGRLP 60
           M     + PGL+GV A  + IS++D Q   +  RG  + +L++  S+LE  +LL+ G LP
Sbjct: 1   MTAVSEFRPGLEGVPATLSSISFVDGQRGVLEYRGISIEQLAQQSSFLETAYLLIWGHLP 60

Query: 61  EESEMETLERKINSASSLPADHLRLLELLPEDTHPMDGLRTGLSALAGY--DRQIDDRSP 118
            + E+   E +I     +      +++  P+  HPMD L+   +AL  +   R +DD  P
Sbjct: 61  TQQELTEFEHEIRYHRRIKFRIRDMMKCFPDSGHPMDALQASAAALGLFYSRRALDD--P 118

Query: 119 SANKERAYQLLGKMPALTAASYRIINKKEPILPLQTLSYSANFLYMMTGKLPSSLEEQIF 178
              +    +LL K+P + AA   I    +PI P   L Y+ANFLYM+T + P  +  +IF
Sbjct: 119 EYIRAAVVRLLAKIPTMVAAFQLIRKGNDPIQPRDELDYAANFLYMLTEREPDPVAARIF 178

Query: 179 DRSLVLYSEHEMPNSTFAARVIASTHSDLYGALTGAVASLKGNLHGGANEAVMYLLLEAK 238
           D  L L++EH +  STF+A V AST +D Y  +  AV +L G LHGGANE V+ +L    
Sbjct: 179 DICLTLHAEHTINASTFSAMVTASTLTDPYAVVASAVGTLAGPLHGGANEEVLDMLEAIG 238

Query: 239 TTSDFEQLLQTKLKRKEKIMGFGHRVYMKKMDPRALMMKEALQQLCDKAGDHRLYEMCEA 298
           +  + E  L   +  K +IMGFGHRVY K  DPRA++++   +QL D  G    YE+  A
Sbjct: 239 SVENVEPYLDHCIATKTRIMGFGHRVY-KVKDPRAVILQNLAEQLFDIFGHDPYYEIAVA 297

Query: 299 GERLMEK---EKGLYPNLDYYAAPVYWMLGIPIPLYTPIFFSARTSGLCAHVIEQHANNR 355
            E+   +    KG+YPN+D+Y+  VY  LGIP  L+TP+F  AR +G  AH  EQ   NR
Sbjct: 298 VEKAAAERLSHKGIYPNVDFYSGLVYRKLGIPSDLFTPVFAIARVAGWLAHWKEQLNENR 357

Query: 356 LFRPRVSYMG 365
           +FRP   Y G
Sbjct: 358 IFRPTQIYTG 367


Lambda     K      H
   0.317    0.134    0.381 

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: 341
Number of extensions: 13
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: 372
Length of database: 386
Length adjustment: 30
Effective length of query: 342
Effective length of database: 356
Effective search space:   121752
Effective search space used:   121752
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 (21.7 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