GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolG in Paraburkholderia bryophila 376MFSha3.1

Align inositol 2-dehydrogenase (EC 1.1.1.18) (characterized)
to candidate H281DRAFT_04465 H281DRAFT_04465 myo-inositol 2-dehydrogenase / D-chiro-inositol 1-dehydrogenase

Query= BRENDA::E1U888
         (350 letters)



>FitnessBrowser__Burk376:H281DRAFT_04465
          Length = 348

 Score =  238 bits (606), Expect = 2e-67
 Identities = 133/341 (39%), Positives = 194/341 (56%), Gaps = 7/341 (2%)

Query: 4   KTIKIGIVGLGRLGKIHATNIATKIQHAKLQAATSVVPAELDWAKKELGVEEVFEDFDDM 63
           + ++ G+VGLGRLGK HA N+A ++  A+L AA S +  E  WA+  L    +++D+  +
Sbjct: 8   RRLRFGVVGLGRLGKRHAENLAYRVPGAELVAACSPLEEERAWARDALPSPRLYDDYARL 67

Query: 64  VQHADIDAVFIVSPSGFHLQQIESALNAGKHVFSEKPIGLDIEAIEHTQQVIAQHANLKF 123
           +   D+DAV++V+PS  H QQI  AL AGKHVF EKP+ LD+   E      AQ+ +L+ 
Sbjct: 68  LDDKDVDAVWLVTPSSLHAQQIVDALRAGKHVFCEKPLSLDLAECERVLHEAAQYPHLQA 127

Query: 124 QLGFMRRFDDSYRYAKQLVDQGKIGDITLIRSYSIDPAAGMASFVKFATSANSGGLFLDM 183
            +GFMRRFD SY+ A   ++ G IG   L+RS + D       FV+FA  A SGG+FLD 
Sbjct: 128 TIGFMRRFDPSYKDAFDKIEAGAIGRPFLVRSQTTDKNDTDGFFVRFA--ATSGGIFLDC 185

Query: 184 SIHDIDVIHWFTGK-EIDKVWAIGLNRAYPVLDKAGELETGAALMQLEDKTMAILVAGRN 242
           ++HDIDV  W  GK    +V+A G    +  L + G+++ G A+ + ED  +A+  A R 
Sbjct: 186 TVHDIDVARWLLGKPRAKRVFAAGAVALHEGLREFGDVDNGVAICEFEDGKLAMFYASRT 245

Query: 243 AAHGYHVETEIIGTKGMLRIAQVPEKNLVTVMNEEGIIRPTSQNFPERFAQAFLSEEQAF 302
            AHG    +E+IGT G L I   P  N V + +  GI    +  F +RF +AFL E +AF
Sbjct: 246 QAHGNDTHSEVIGTAGGLTIGHNPRANRVEIYDATGIRNECTPGFFDRFEEAFLHEARAF 305

Query: 303 VNSILNNQ----DVGITAEDGLQGTKAALALQEAFEKNDIV 339
           V S+          G T  D L+ T+   AL+++ +    V
Sbjct: 306 VASVQGGAGSAVQAGATLADALEATRIGNALRQSLQSGQAV 346


Lambda     K      H
   0.318    0.134    0.377 

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: 313
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: 350
Length of database: 348
Length adjustment: 29
Effective length of query: 321
Effective length of database: 319
Effective search space:   102399
Effective search space used:   102399
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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