GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Pantoea rwandensis LMG 26275

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate WP_084934899.1 HA51_RS12950 ABC transporter ATP-binding protein

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



>NCBI__GCF_002095475.1:WP_084934899.1
          Length = 367

 Score =  244 bits (624), Expect = 2e-69
 Identities = 144/367 (39%), Positives = 207/367 (56%), Gaps = 30/367 (8%)

Query: 1   MSALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60
           MS L + +I K +GE   L  I      G F+ LLG SGCGKSTLL  IAGL     G+I
Sbjct: 1   MSHLSLHHITKAWGEKIALNDISFDAAEGSFVALLGPSGCGKSTLLRTIAGLETADSGEI 60

Query: 61  LIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARL 120
                 +  + P  R ++MVFQSYAL+P+L+V  N+ FGL+ R   +      + D ++L
Sbjct: 61  HFKHSDITHLPPSQRKLSMVFQSYALFPHLNVRENLLFGLKARGEDKQTFTTRLDDVSKL 120

Query: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180
           ++++ LLDR PSQLSGGQ+QRVA+GRA++ N  + L DEPLSNLDAKLR  MR E++ L 
Sbjct: 121 MELDKLLDRLPSQLSGGQQQRVALGRAVIANNNLCLMDEPLSNLDAKLRQSMRREIRALQ 180

Query: 181 QMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMN 240
           + L  T++YVTHDQ EAM++A  I ++ DG IEQ   P+++Y+ PAT++ A F+G+PPMN
Sbjct: 181 KKLALTMLYVTHDQTEAMSMADSIILLNDGHIEQHGTPNDLYNNPATIFAAQFIGAPPMN 240

Query: 241 ILDAEMTANGLK----------IEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAG 290
           IL   + A G +          +E C+EV                + +G+R E ++L + 
Sbjct: 241 IL--PLHAKGEQHYLSHLQTPVVERCDEV---------------ALSLGLRAEDIQLISA 283

Query: 291 SEAQRLTASVEVVELTGPELVTTATVG--SQRITACLPPRTAVGMGSAHAFTFDGTALHL 348
             A  LTA V   E  G + +    +   S+ +T  +P       GS     +     +L
Sbjct: 284 DNA-ALTARVISYEYMGSDTLLACQLAGLSELVTVKVPGMQRYDEGSLVGLQWSAARQYL 342

Query: 349 FDPESGR 355
           F   SG+
Sbjct: 343 FSSTSGK 349


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: 268
Number of extensions: 10
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: 367
Length adjustment: 29
Effective length of query: 331
Effective length of database: 338
Effective search space:   111878
Effective search space used:   111878
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 24 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