GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aapJ in Sinorhizobium meliloti 1021

Align ABC transporter for L-Glutamine, L-Histidine, and other L-amino acids, periplasmic substrate-binding component (characterized)
to candidate SMc00676 SMc00676 amino acid-binding periplasmic signal peptide protein

Query= reanno::Smeli:SMc02118
         (341 letters)



>FitnessBrowser__Smeli:SMc00676
          Length = 331

 Score =  402 bits (1033), Expect = e-117
 Identities = 190/320 (59%), Positives = 243/320 (75%), Gaps = 2/320 (0%)

Query: 22  ASAATLDDVKAKGFVQCGVNTGLAGFAAPDASGNWSGFDVDYCKAIAAAIFGDGSKVKYT 81
           A AATLD VK +G ++CGV+ G+ GF+APD  G WSGFD+D+C+A+AAA  G   KVKY 
Sbjct: 14  AQAATLDVVKQRGELRCGVSQGVLGFSAPDDKGEWSGFDIDFCRAVAAATLGSPDKVKYV 73

Query: 82  PLSAKERFPALQSGEVDVLARNTTWSINRDTALGFNFRPVNYYDGQGFMVRKELDVKSAL 141
           PLS KERF ALQSGEVD+L+R TTW+++RDT LG +F  VNYYDGQ FMVR ++ VKS  
Sbjct: 74  PLSTKERFTALQSGEVDLLSRQTTWTLSRDTDLGMSFVGVNYYDGQAFMVRGDIGVKSVK 133

Query: 142 ELSGAAVCVQTGTTTELNLADYFKANNLQYNPVVFEKLEEVNAAYDAGRCDVYTTDQSGL 201
           ELSGA+VC +TGTTTE N+ADYF AN ++Y  + FEK ++   A+++GRCDVY+TD S L
Sbjct: 134 ELSGASVCTETGTTTEQNMADYFSANKIEYQVIAFEKADQTIQAFNSGRCDVYSTDASAL 193

Query: 202 YSLRLTLSKPDDHIVLPEIISKEPLAPAVRQGDDQWFDIVSWVHYALVQAEEFGVTQANL 261
           YS RLTL+ PD  +VLPE+ISKEPL PAVRQGDDQWF +V W  +A+++AEE G+T+ N 
Sbjct: 194 YSQRLTLNDPDRFVVLPEVISKEPLGPAVRQGDDQWFKVVRWTLFAMIEAEELGITRENA 253

Query: 262 EEMKKSTNPDVQRFLGVEADSKIGTDLGLTNEWAVNIVKAVGNYGEVFDRNIGAGSPLKI 321
             + +S     +RFLG+  D++ G  LGL  +WA   V AVGNYGE+F+R++G  S L+I
Sbjct: 254 ASLLESGTAAQKRFLGI--DNEAGKALGLDPKWAYQTVAAVGNYGEIFERHLGKESALRI 311

Query: 322 ERGLNALWNKGGLQYAPPVR 341
           +RGLN LWN GGL YAPPVR
Sbjct: 312 DRGLNKLWNNGGLIYAPPVR 331


Lambda     K      H
   0.317    0.134    0.399 

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: 379
Number of extensions: 15
Number of successful extensions: 2
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: 341
Length of database: 331
Length adjustment: 28
Effective length of query: 313
Effective length of database: 303
Effective search space:    94839
Effective search space used:    94839
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 (21.6 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