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_0947 Synpcc7942_0947 ATPase

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



>FitnessBrowser__SynE:Synpcc7942_0947
          Length = 355

 Score =  282 bits (722), Expect = 8e-81
 Identities = 156/357 (43%), Positives = 226/357 (63%), Gaps = 8/357 (2%)

Query: 3   ALEIRNIRKRYG-EVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDIL 61
           ALE+R +RK Y   V  +  + + L+ GEFL LLG SGCGKST L +IAGL +P+ G I 
Sbjct: 5   ALELRQLRKAYSPSVVPVANLSLQLQPGEFLTLLGPSGCGKSTTLRLIAGLDQPTSGSIW 64

Query: 62  IGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARLL 121
           +G+R +  + P DRD+AMVFQSYALYP+L+V +N+  GL++RR   AE ++ ++  A  L
Sbjct: 65  LGDREITTLPPGDRDMAMVFQSYALYPHLNVRQNLTLGLQIRRTSAAEIEQRLQQVAHNL 124

Query: 122 QIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLHQ 181
           ++++LLDR+P+QLSGGQRQRVA+GRALVR P VFL DEPLSNLDA LR ++R ++K L  
Sbjct: 125 ELDHLLDRRPAQLSGGQRQRVALGRALVRQPSVFLLDEPLSNLDALLREQVRAQMKALFS 184

Query: 182 MLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMNI 241
              + VVYVTHDQ EA++L+ RIA++  G ++QL +PD +Y  PA  +VAGF+GSP MN+
Sbjct: 185 QQASPVVYVTHDQTEALSLSHRIAILNGGHLQQLDSPDRIYQAPANAFVAGFIGSPRMNL 244

Query: 242 LDAEMTANGLKIEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAGSEAQRLTASVE 301
           L   + +    +      LP+P+       A  +V  G+RPE L+LA     + +   + 
Sbjct: 245 LPLPIHSGQAWLG--SRALPIPSHLA----ARSQVLWGLRPEHLKLATPEVERAIPVQLH 298

Query: 302 VVELTGPE-LVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESGRSL 357
           + E  G + L+T A   +  +   L   +   + +    TF+  + H F P +G  L
Sbjct: 299 LTENLGMQRLLTVAIAANPEVRLRLLMPSDQPIPTDLQVTFEPESQHWFCPSTGDRL 355


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: 345
Number of extensions: 15
Number of successful extensions: 1
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: 355
Length adjustment: 29
Effective length of query: 331
Effective length of database: 326
Effective search space:   107906
Effective search space used:   107906
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