GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Sinorhizobium fredii NGR234

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate WP_015887278.1 NGR_RS05625 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

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



>NCBI__GCF_000018545.1:WP_015887278.1
          Length = 360

 Score =  583 bits (1504), Expect = e-171
 Identities = 310/362 (85%), Positives = 325/362 (89%), Gaps = 6/362 (1%)

Query: 1   MSALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60
           MSALEIRNIRKRYG+VETLK IDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI
Sbjct: 1   MSALEIRNIRKRYGDVETLKSIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60

Query: 61  LIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARL 120
           LIGERS+LG HPKDRDIAMVFQSYALYPN+SVARNIGFGLEMR+VP AE +KAVRDTARL
Sbjct: 61  LIGERSILGAHPKDRDIAMVFQSYALYPNMSVARNIGFGLEMRKVPAAEREKAVRDTARL 120

Query: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180
           LQIENLLDRKPSQLSGGQRQRVAIGRALVR PQVFLFDEPLSNLDAKLRMEMRTELKRLH
Sbjct: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVREPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180

Query: 181 QMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMN 240
           QML+TTVVYVTHDQIEAMTLATRIAVMRDGRIEQL  P E+YDRPATLYVAGFVGSPPMN
Sbjct: 181 QMLKTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLGTPAEIYDRPATLYVAGFVGSPPMN 240

Query: 241 ILDAEMTANGLKIEGCEEVLPLPAAF-NGAAWAGRRVKVGIRPEALRLAAGSEAQ--RLT 297
           ILDAE T +GL+I G E  LPL  AF NG    GRRVKVGIRPEALRL AG +A   RLT
Sbjct: 241 ILDAEGTGSGLRILGSENTLPLGGAFPNGT--TGRRVKVGIRPEALRL-AGDDATGGRLT 297

Query: 298 ASVEVVELTGPELVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESGRSL 357
           A VEV+ELTGPELV TA +G QRITACLPPRT++  GS  AF+FD  ALHLFDPESG SL
Sbjct: 298 AIVEVMELTGPELVITARIGEQRITACLPPRTSLEPGSTQAFSFDEAALHLFDPESGLSL 357

Query: 358 RM 359
           RM
Sbjct: 358 RM 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: 517
Number of extensions: 9
Number of successful extensions: 3
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: 360
Length adjustment: 29
Effective length of query: 331
Effective length of database: 331
Effective search space:   109561
Effective search space used:   109561
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 Apr 09 2024. 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