GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Phaeobacter inhibens BS107

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 GFF3769 PGA1_262p01730 putative glutathione import ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__Phaeo:GFF3769
          Length = 325

 Score =  195 bits (495), Expect = 1e-54
 Identities = 120/336 (35%), Positives = 187/336 (55%), Gaps = 17/336 (5%)

Query: 1   MKEILLKAENVRAYYKLEKVSVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMV 60
           M E LL+ +++   Y+  +  +KA+  +SF++ + E++G+VGESGCGK+TL + I   + 
Sbjct: 1   MSEKLLEIDDLSVDYETARGDLKALRSISFDVNKGEIVGIVGESGCGKSTLISAILRLIA 60

Query: 61  KPLTLVDGKIFLRVNGEFVELSSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRMEKYVR 120
                 +G++  R  GE + ++S   D   R   G +I+I+ Q  M    P I + K + 
Sbjct: 61  PNTRFRNGEV--RFKGEDLLVAS---DRHIRDLRGDDISIVFQDPMQTHNPVISIGKQMV 115

Query: 121 HLAESHGIDEEELLDKARRRFEEVGL-DP-LWIKRYPFELSGGMRQRAVIAIATILNPSL 178
            +       + E L  A +    VG+ DP + +K+YP E SGGMRQR  IA+A +  P L
Sbjct: 116 DIQHRSKASKAEKLATAAKMLGAVGIPDPEMRLKQYPHEFSGGMRQRIAIAMALMSEPDL 175

Query: 179 LIADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGKIV 238
           LIADEPT+ALD   +  +++ L +++ +    +I+FI+H +  + ++ DR+++MYAG +V
Sbjct: 176 LIADEPTTALDATLEVQIIERLKELQSE-FGCAILFISHHLGVIAELCDRVVVMYAGAVV 234

Query: 239 EFAPVESLLEKPLHPYTQGLFNSVLTPEP---EVKKRGITTIPGAPPNLINPPSGCRFHP 295
           E   V  +   P HPYT+ L       +P   + + R + TIPG  P+L N P GC F  
Sbjct: 235 ESGTVREIFHNPKHPYTRRLIEC----DPGHLKERARVLPTIPGEVPDLANLPEGCIFRD 290

Query: 296 RCPHAMDVCKEKEPPLTEIEPGRRVACWL-YMEERA 330
           RC  AMD C    PPL  +  G   ACWL + EE A
Sbjct: 291 RCDQAMDRC-ASVPPLARLSEGHNAACWLNHAEEMA 325


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: 260
Number of extensions: 8
Number of successful extensions: 6
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: 325
Length adjustment: 28
Effective length of query: 302
Effective length of database: 297
Effective search space:    89694
Effective search space used:    89694
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: 48 (23.1 bits)

This GapMind analysis is from Sep 17 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