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_061942552.1 CPter91_RS17900 sn-glycerol-3-phosphate import ATP-binding protein UgpC

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



>NCBI__GCF_001584185.1:WP_061942552.1
          Length = 359

 Score =  332 bits (851), Expect = 9e-96
 Identities = 177/363 (48%), Positives = 244/363 (67%), Gaps = 9/363 (2%)

Query: 1   MSALEIRNIRKRYGE----VETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPS 56
           M+ + ++N++K YG+    V+ + GI I +  GEF+V++G SGCGKSTLL ++AGL E S
Sbjct: 1   MAQVHLKNVKKTYGKAPKAVDVIHGISIDIADGEFIVMVGPSGCGKSTLLRMVAGLEEVS 60

Query: 57  GGDILIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRD 116
            GDI+IGER V  + PKDRDIAMVFQ+YALYP++SV  N+ +GL++R + + + +  V+ 
Sbjct: 61  AGDIVIGERVVNQLEPKDRDIAMVFQNYALYPHMSVYENMAYGLKIRGLSKDDIETRVQK 120

Query: 117 TARLLQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTEL 176
            A++L++  LL R P QLSGGQRQRVA+GRA+VR P VFLFDEPLSNLDAKLR++MR E+
Sbjct: 121 AAKILELGALLQRTPRQLSGGQRQRVAMGRAIVREPAVFLFDEPLSNLDAKLRVQMRLEI 180

Query: 177 KRLHQMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGS 236
           ++LH+ L TT +YVTHDQ+EAMTL  R+ VM  GR EQ+  P EVY RPAT +VA F+GS
Sbjct: 181 QKLHRTLGTTSLYVTHDQVEAMTLGQRMIVMNGGRAEQIGTPAEVYARPATTFVASFIGS 240

Query: 237 PPMNILDAEMTANGLKIEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAGSEAQRL 296
           PPMN+L   + A+G      +    +   F+    AGR   +G+RPE  +L  G     L
Sbjct: 241 PPMNLLCGRVAADGNSF-AIDNAAAVSLPFSCHPIAGRDCIMGLRPE--QLIFGQPGLNL 297

Query: 297 TASVEVVELTGPELVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESGRS 356
            A  E+VE  G +L+   ++G Q +   +P  TAV  G      FD  ALH FDPE+ + 
Sbjct: 298 RA--ELVEALGADLLVHVSIGDQLLVMRVPAATAVEAGQQITAGFDAAALHWFDPETTQR 355

Query: 357 LRM 359
           + +
Sbjct: 356 IEL 358


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: 359
Number of extensions: 16
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: 359
Length adjustment: 29
Effective length of query: 331
Effective length of database: 330
Effective search space:   109230
Effective search space used:   109230
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