GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Synechococcus elongatus PCC 7942

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate Synpcc7942_0960 Synpcc7942_0960 ATPase

Query= reanno::Smeli:SM_b21216
         (360 letters)



>FitnessBrowser__SynE:Synpcc7942_0960
          Length = 417

 Score =  286 bits (732), Expect = 7e-82
 Identities = 169/373 (45%), Positives = 229/373 (61%), Gaps = 30/373 (8%)

Query: 14  GEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDILIGERSVLGVHPK 73
           GEV  L GI++ +  GEF+V++G SGCGKSTLL ++AGL  PS G I +G+R V  +  K
Sbjct: 45  GEVVVLNGINLEIADGEFMVVVGPSGCGKSTLLRLLAGLETPSRGLIKVGDRRVDRLPAK 104

Query: 74  DRDIAMVFQSYALYPNLSVARNIGFGLEM---------------RRVP---------QAE 109
            RDIAMVFQSYALYP+LSV  N+ FGL                 R +P         +A 
Sbjct: 105 ARDIAMVFQSYALYPHLSVYDNLAFGLRRQGDRPWWQQQLALATRSLPKSLQYEPEQEAR 164

Query: 110 HDKAVRDTARLLQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLR 169
             + VR+ A +LQ++ LLDR+P QLSGGQ+QRVA+GRA+ RNPQVFL DEPLSNLDAKLR
Sbjct: 165 IKRRVREVATMLQLDTLLDRQPKQLSGGQKQRVALGRAIARNPQVFLMDEPLSNLDAKLR 224

Query: 170 MEMRTELKRLHQMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLY 229
            E R ++  L + L  T +YVTHDQ EAMT+  RIAV+  G ++Q+A+P E+YDRPA  +
Sbjct: 225 AETRAQIVSLQRQLGVTTLYVTHDQTEAMTMGDRIAVLNRGHLQQVASPLEIYDRPANRF 284

Query: 230 VAGFVGSPPMNILDAEMTANGLKIEGCEEVLPLPAAFNGA--AWAGRRVKVGIRPEALRL 287
           VA F+GSPPMN++   + A  L++        LP A+      + G+ V++GIRPE L +
Sbjct: 285 VAQFIGSPPMNLIPVTVRA-PLQLTTENFRCTLPEAWEPVLRLYDGQTVELGIRPEHLEV 343

Query: 288 AAGSEAQRLTASVEVVELTGPELVTTATVGSQRIT--ACLPPRTAVGMGSAHAFTFDGTA 345
            A + ++ L  +V  VE  G +      +    I   A L P+    MG     TF    
Sbjct: 344 GAAA-SKNLLITVTGVEALGSDTFIAGELKESGIAVQARLAPQQCWQMGDRLWLTFKPDQ 402

Query: 346 LHLFDPESGRSLR 358
           +HLFD E+G+++R
Sbjct: 403 IHLFDLETGKAIR 415


Lambda     K      H
   0.320    0.136    0.385 

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: 389
Number of extensions: 11
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: 360
Length of database: 417
Length adjustment: 30
Effective length of query: 330
Effective length of database: 387
Effective search space:   127710
Effective search space used:   127710
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: 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