GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Magnetospirillum magneticum AMB-1

Align 3-hydroxyisobutyryl-CoA hydrolase, mitochondrial; 3-hydroxyisobutyryl-coenzyme A hydrolase; HIB-CoA hydrolase; HIBYL-CoA-H; EC 3.1.2.4 (characterized)
to candidate WP_011384942.1 AMB_RS12890 enoyl-CoA hydratase/isomerase family protein

Query= SwissProt::Q5XIE6
         (385 letters)



>NCBI__GCF_000009985.1:WP_011384942.1
          Length = 352

 Score =  276 bits (705), Expect = 8e-79
 Identities = 156/351 (44%), Positives = 213/351 (60%), Gaps = 8/351 (2%)

Query: 36  EVLLERRGCAGVITLNRPKLLNALSLNMIRQIYPQLKKWERDPDTFLIIIKGAGGKAFCA 95
           E L+   G  G I LNRPK+LNALS      I   L  WE DPD  +I+I+G G +AFCA
Sbjct: 4   ETLISSGGRLGRIVLNRPKVLNALSARQYHDITACLVSWESDPDVAVILIEGEGERAFCA 63

Query: 96  GGDIKALSEAKKAGQT-LSQDLFREEYILNNAIASCQKPYVALIDGITMGGGVGLSVHGQ 154
           GGDI+ + +A + G +  S D+FR EY LN  I +  KPYV+++DGI MGGG  LSV+G+
Sbjct: 64  GGDIRMVWDAARRGDSEFSHDVFRTEYRLNRRIHAYPKPYVSVLDGICMGGGARLSVNGR 123

Query: 155 FRVATERSLFAMPETGIGLFPDVGGGYFLPRLQGKLGYFLALTGFRLKGRDVHRAGIATH 214
           FRVATER+ FAMPETGIG FPDVG  +FL R  G LG +L LTG +L   D   AGIATH
Sbjct: 124 FRVATERTRFAMPETGIGFFPDVGATHFLNRCPGDLGLYLGLTGKQLGPADCLWAGIATH 183

Query: 215 FVDSEKLHVLEEEL-LALKSPSAED-VAGVLESYHAKSKMGQDKSIIFEEHMDKINSCFS 272
           FV + ++  L   L +A +S   ED V  VL  +H     G         HM+ +  CF+
Sbjct: 184 FVPAARVDDLRAGLRVAAQSADPEDAVEDVLARFHQPVADGP-----LVRHMEALERCFA 238

Query: 273 ANTVEQILENLRQDGSPFAMEQIKVINKMSPTSLKITLRQLMEGSTKTLQEVLTMEYRLT 332
              ++ ++E LR DG  +A + I  ++  +P SL +TLRQL EG      + +  E+RLT
Sbjct: 239 PRRLDDMIEALRLDGGQWAWDTIWELSGRAPFSLAVTLRQLREGRGMGFDDAIRREFRLT 298

Query: 333 QACMEGHDFHEGVRAVLIDKDQTPKWKPADLKDVTDEDLNSYFKSLGSRDL 383
              + G DF EG+RA ++DKD+ P W P+ L +V +  + + F++LG  +L
Sbjct: 299 WRFLLGQDFLEGIRAQVVDKDRRPNWSPSSLAEVDELAVAACFQTLGDDEL 349


Lambda     K      H
   0.320    0.136    0.394 

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: 341
Number of extensions: 12
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: 385
Length of database: 352
Length adjustment: 30
Effective length of query: 355
Effective length of database: 322
Effective search space:   114310
Effective search space used:   114310
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 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