GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylH in Pseudovibrio axinellae Ad2

Align Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized)
to candidate WP_068009667.1 PsAD2_RS19325 ribose ABC transporter permease

Query= TCDB::G4FGN4
         (313 letters)



>NCBI__GCF_001623255.1:WP_068009667.1
          Length = 314

 Score =  223 bits (567), Expect = 6e-63
 Identities = 127/300 (42%), Positives = 182/300 (60%), Gaps = 9/300 (3%)

Query: 17  LIAIVVFLGVTTREFLTVENIFTVILNVSFIAIMSFGMTMVIITSGIDLSVGSILGAASV 76
           LI ++  +      FL V+N+  ++   S  A+++ GMT VI+TSGIDLSVGSIL  A  
Sbjct: 16  LIILMAAVSFANANFLGVDNMLNILRQTSINAVIAMGMTFVILTSGIDLSVGSILAFAGA 75

Query: 77  VMGLLMDEKGLSPFLSVVI--GLAVGVGFGLANGLLITKARLAPFISTLGMLSVGRGLAY 134
           +   L+   G+   L V +   + VG G G  +G++I+   + PFI+TL  +++ RG   
Sbjct: 76  ICASLI---GMDTPLVVALFATIMVGAGLGATSGVIISYFNVQPFIATLVGMTMIRGATL 132

Query: 135 VMSGGWPISP----FPESFTVHGQGMVGPVPVPVIYMAVIGVIAHIFLKYTVTGRRIYAI 190
           V + G P+S       ESF   G G +  +P PVI M VI  I    L  T  GR +YAI
Sbjct: 133 VYTQGRPVSTGSHDVAESFYQFGAGYIFGIPHPVILMIVIFAICWFILSQTRFGRYVYAI 192

Query: 191 GGNMEASKLVGIKTDRILILVYTINGFLAAFAGFLLTAWLGVAQPNAGQGYELDVIAATV 250
           GGN   ++L GI   ++ ILVY ++G LAA AG +LTA L  AQP AG GYELD IAA V
Sbjct: 193 GGNENVARLSGINVKKVKILVYALSGALAALAGIILTARLESAQPTAGLGYELDAIAAVV 252

Query: 251 IGGTSLSGGEGTILGAFLGAVIMGVLRNGMILLGVSSFWQQVVIGIVIIIAIAIDQIRRA 310
           +GGTSL+GG+G + G  +GA+I+GVL N + ++ VSS++Q +  G VI++A+ +D   +A
Sbjct: 253 LGGTSLAGGKGRVFGTIIGALIIGVLNNALNIMDVSSYYQMIAKGAVILLAVVVDSRGKA 312


Lambda     K      H
   0.328    0.145    0.421 

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: 290
Number of extensions: 21
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: 313
Length of database: 314
Length adjustment: 27
Effective length of query: 286
Effective length of database: 287
Effective search space:    82082
Effective search space used:    82082
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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