GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Rhizobium leguminosarum 3841

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate WP_011653645.1 RL_RS21900 ABC transporter ATP-binding protein

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



>NCBI__GCF_000009265.1:WP_011653645.1
          Length = 371

 Score =  358 bits (920), Expect = e-103
 Identities = 198/366 (54%), Positives = 254/366 (69%), Gaps = 13/366 (3%)

Query: 1   MSALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60
           M+ LEI  ++KR+G V+ LKGID+ LE G FLVL+G SGCGKSTLLN IAGL   + GDI
Sbjct: 1   MAFLEISGLKKRFGAVDILKGIDLELEKGGFLVLVGPSGCGKSTLLNTIAGLETITSGDI 60

Query: 61  LIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARL 120
            I  R + G+HP  RDIAMVFQSYALYPN++VA NI FG+E+R VP+ E  +A+   + +
Sbjct: 61  KIDGRDISGLHPSKRDIAMVFQSYALYPNMTVAGNIAFGMEIRGVPKEERARAIAQVSDM 120

Query: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180
           LQI +LLDRKPSQLSGGQRQRVA+GRALVRNPQVFLFDEPLSNLDAKLR++MRTE+KRLH
Sbjct: 121 LQIGHLLDRKPSQLSGGQRQRVAMGRALVRNPQVFLFDEPLSNLDAKLRVDMRTEIKRLH 180

Query: 181 QMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMN 240
           Q + TT VYVTHDQIEAMTLAT+IAV++DG ++Q   P E+Y+ P+ ++VA F+GSP MN
Sbjct: 181 QRMGTTFVYVTHDQIEAMTLATKIAVLKDGVLQQFGTPAEIYNSPSNIFVADFMGSPAMN 240

Query: 241 ILDA--EMTANGLKI-----EGCEEVLPLPAAFNG-AAWAGRRVKVGIRPEALRLAAGSE 292
           +L+A  E  A GL++           LP+ +  +G  A+ G++V  GIRPEAL    G++
Sbjct: 241 LLNATVENGAGGLEVSLERPNAAPLRLPVISGNDGLTAYTGKQVIFGIRPEALTDPDGAD 300

Query: 293 --AQRLTAS---VEVVELTGPELVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALH 347
             A+ LT     +EVVE  G +      +G + + A L   T +  G      F+     
Sbjct: 301 RKARSLTEGDCLIEVVEPAGSDTFAVTKLGGKSVVARLRADTGIAPGQNTRLAFNLDKAV 360

Query: 348 LFDPES 353
            FDP S
Sbjct: 361 FFDPNS 366


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: 372
Number of extensions: 14
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: 371
Length adjustment: 30
Effective length of query: 330
Effective length of database: 341
Effective search space:   112530
Effective search space used:   112530
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