GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Collimonas pratensis Ter91

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate WP_061939852.1 CPter91_RS10210 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

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



>NCBI__GCF_001584185.1:WP_061939852.1
          Length = 363

 Score =  291 bits (746), Expect = 1e-83
 Identities = 159/362 (43%), Positives = 227/362 (62%), Gaps = 8/362 (2%)

Query: 1   MSALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60
           M+++    + K Y     +    + +   EF+VLLG SGCGKST+L ++AGL E SGG +
Sbjct: 1   MASIVCDKLVKHYEGNPVVHDFSMEIADAEFIVLLGPSGCGKSTILRMMAGLEEISGGAL 60

Query: 61  LIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARL 120
            IG R V  + P++RDIAMVFQ+Y LYP+++V  N+ FGL   + P++E  + V   A++
Sbjct: 61  HIGARQVNDLPPRERDIAMVFQNYVLYPHMTVYDNMAFGLRRLKTPESEISQRVGQVAQM 120

Query: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180
           L +E LL RKP Q+SGGQ+QRVAIGRA+++ P VFLFDEPLSNLDAKLR ++R ++KRLH
Sbjct: 121 LSLEPLLQRKPKQMSGGQQQRVAIGRAMIKTPAVFLFDEPLSNLDAKLRAQLRGDIKRLH 180

Query: 181 QMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMN 240
           + L TT VYVTHDQ+EAMTLA RI +++ GRIEQ+  P E+Y+ P + + AGF+G+P MN
Sbjct: 181 RQLATTSVYVTHDQLEAMTLADRIVLLKAGRIEQVGTPAEIYNHPVSRFAAGFIGTPAMN 240

Query: 241 ILDAEMT-ANGLKIEGCEEV---LPLPAAFNGAAWAGRRVKVGIRPEAL-RLAAGSEAQR 295
            +    +  +G+ +    E    LP P+ F  A   G+ V +G+RP  +   + G     
Sbjct: 241 FIGCVASHEDGMTVLDSGEARWRLP-PSLF--AVSEGQSVVLGVRPNHMFTTSVGDRQIE 297

Query: 296 LTASVEVVELTGPELVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESGR 355
           +   V++VEL G E + +       ITA +P      +G    F      LH+FD E+G 
Sbjct: 298 VRGKVDLVELLGAESLVSLLHAKHEITALVPANRCPRVGDQVCFNISLNDLHVFDAETGS 357

Query: 356 SL 357
           SL
Sbjct: 358 SL 359


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: 350
Number of extensions: 14
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: 360
Length of database: 363
Length adjustment: 29
Effective length of query: 331
Effective length of database: 334
Effective search space:   110554
Effective search space used:   110554
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