GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdA in Synechococcus elongatus PCC 7942

Align 2-oxoisovalerate dehydrogenase subunit alpha; Branched-chain alpha-keto acid dehydrogenase E1 component alpha chain; BCKDH E1-alpha; EC 1.2.4.4 (characterized)
to candidate Synpcc7942_1944 Synpcc7942_1944 Pyruvate dehydrogenase (lipoamide)

Query= SwissProt::Q5SLR4
         (367 letters)



>FitnessBrowser__SynE:Synpcc7942_1944
          Length = 342

 Score =  176 bits (446), Expect = 8e-49
 Identities = 111/320 (34%), Positives = 163/320 (50%), Gaps = 10/320 (3%)

Query: 40  RLYRDMLAARMLDERYTILIRTGKT-SFIAPAAGHEAAQVAIAHAIRPGFDWVFPYYRDH 98
           R+Y DM+  R  +++   +   GK   F+    G EA    I  A+R   D+V   YRDH
Sbjct: 24  RIYEDMVLGRTFEDKCAEMYYRGKMFGFVHLYNGQEAVASGIIKAMRSD-DYVCSTYRDH 82

Query: 99  GLALALGIPLKELLGQMLATKADPNKGRQMPEHPGSKALNFFTVASPIASHVPPAAGAAI 158
             AL+ G+P ++++ ++   +   ++GR    H  S   N     + +A  +P A GAA 
Sbjct: 83  VHALSAGVPARQVMAELFGKETGCSRGRGGSMHLFSAEHNLLGGFAFVAEGIPVATGAAF 142

Query: 159 SMKLLRTG-------QVAVCTFGDGATSEGDWYAGINFAAVQGAPAVFIAENNFYAISVD 211
           +    R         QV  C FGDGA + G ++  +N A +   P +F+ ENN +AI + 
Sbjct: 143 TTAYRRNALGDTSADQVTACFFGDGAANNGQFFECLNMATLWKLPILFVVENNKWAIGMS 202

Query: 212 YRHQTHSPTIADKAHAFGIPGYLVDGMDVLASYYVVKEAVERARRGEGPSLVELRVYRYG 271
           +   T  P I  K  AFG+PG  VDGMDVLA   V +EA+ RAR GEGP+L+E   YR+ 
Sbjct: 203 HERATSDPEIYKKGPAFGMPGVEVDGMDVLAVRAVAQEAIARARAGEGPTLIEALTYRFR 262

Query: 272 PHSSADDDSRYRPKEEVAFWRKKDPIPRFRRFLEARGLWNEEWEEDVREEIRAELERGLK 331
            HS AD D   R KEE  FW  +DPI RF   L    L   E  + + ++I A +   ++
Sbjct: 263 GHSLADPD-ELRSKEEKEFWLARDPIKRFAAHLTEFNLATHEELKAIDKKIEALVAEAVE 321

Query: 332 EAEEAGPVPPEWMFEDVFAE 351
            A  +    PE +   ++AE
Sbjct: 322 FAISSPEPKPEELTRYIWAE 341


Lambda     K      H
   0.320    0.137    0.421 

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: 350
Number of extensions: 20
Number of successful extensions: 3
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: 367
Length of database: 342
Length adjustment: 29
Effective length of query: 338
Effective length of database: 313
Effective search space:   105794
Effective search space used:   105794
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