GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Pandoraea thiooxydans ATSB16

Align TM0028, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate WP_156884823.1 PATSB16_RS03180 ATP-binding cassette domain-containing protein

Query= TCDB::Q9WXN5
         (330 letters)



>NCBI__GCF_001931675.1:WP_156884823.1
          Length = 330

 Score =  174 bits (440), Expect = 4e-48
 Identities = 114/344 (33%), Positives = 181/344 (52%), Gaps = 30/344 (8%)

Query: 1   MKEILLKAENVRAYYKL------------EKVSVKAVDGLSFEILEDEVIGVVGESGCGK 48
           M E L+K ++   Y+ +            ++ +++AVDG+SF+I   E + +VGESGCGK
Sbjct: 1   MHEPLVKVDDAARYFDVSASWLDRLLQGKQRSTLRAVDGVSFDIARGETLALVGESGCGK 60

Query: 49  TTLSNVIFMNMVKPLTLVDGKIFLRVNGEFVELSSMTRDEVKRKFWGKEITIIPQAAMNA 108
           +T++ ++    V    L  G I      E   ++++   E +     + + +I Q    +
Sbjct: 61  STIARLL----VGLYGLTRGAIHF----EGQPIAALATREGRHL--RQRLQMIFQDPYAS 110

Query: 109 LMPTIRMEKYVRHLAESHGID--EEELLDKARRRFEEVGLDPLWIKRYPFELSGGMRQRA 166
           L P  R+ + +    ++H  D    E+  +       VGL+     +YP + SGG RQR 
Sbjct: 111 LDPRWRVGRIIAEPLQAHCPDMSRAEMEQRVDELLGLVGLNAADKVKYPHQFSGGQRQRI 170

Query: 167 VIAIATILNPSLLIADEPTSALDVVNQKVLLKVLMQMK-RQGIVKSIIFITHDIATVRQI 225
            IA A    P  L+ DEPTSALDV  Q  +L ++  ++ R G+  + +FI+H++A V  I
Sbjct: 171 SIARALATQPEFLVCDEPTSALDVSVQAQVLNLMKDLQQRMGL--TYLFISHNLAVVHHI 228

Query: 226 ADRMIIMYAGKIVEFAPVESLLEKPLHPYTQGLFNSVLTPEPEVKKRGITTIPGAPPNLI 285
           ADR+ +MY G++VE AP   L   P HPYT+ L +++  P+  +  +  T + G  PN +
Sbjct: 229 ADRVGVMYLGRMVEIAPKRELFAHPRHPYTRMLLDAI--PDLNMTGKARTPVAGEVPNPL 286

Query: 286 NPPSGCRFHPRCPHAMDVCKEKEPPLTEIEPGRRVACWLYMEER 329
           NPP GC FHPRCPHA + C+ +E P   +     VAC    E R
Sbjct: 287 NPPPGCTFHPRCPHANERCR-REAPAPLLHGATTVACHAVQEAR 329


Lambda     K      H
   0.321    0.138    0.405 

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: 311
Number of extensions: 20
Number of successful extensions: 4
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: 330
Length of database: 330
Length adjustment: 28
Effective length of query: 302
Effective length of database: 302
Effective search space:    91204
Effective search space used:    91204
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