GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuC in Acidovorax sp. GW101-3H11

Align 3-hydroxy-3-methylglutaryl-coenzyme A lyase/3-methylglutaconyl-coenzyme A hydratase; EC 4.1.3.4; EC 4.2.1.18 (characterized)
to candidate Ac3H11_199 Hydroxymethylglutaryl-CoA lyase (EC 4.1.3.4)

Query= CharProtDB::CH_122457
         (599 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_199
          Length = 349

 Score =  183 bits (465), Expect = 9e-51
 Identities = 124/311 (39%), Positives = 171/311 (54%), Gaps = 17/311 (5%)

Query: 7   TVRIVEVGPRDGLQNIPQSIDSTIKLDLIRRLRDAGLQTIELTSFVSPRAIPQLADAQVV 66
           TVR  EVG RDGLQ+I   + +  K++ +     AG + IE+ SFV  R +PQLAD   V
Sbjct: 42  TVR--EVGLRDGLQSIATVVSTAQKIEWLNAAYAAGQREIEVGSFVPARLLPQLADTADV 99

Query: 67  VQNADIQKLLKNPKLRLPVLVPNLKGLERALHNGIKEVAVFISATEGFSRANINCTVDEG 126
           + +A   K L  P L   VLVPN+KG ERAL  G   + V +SA+   S AN+  T DE 
Sbjct: 100 LAHA---KTL--PGLVASVLVPNVKGAERALECGADLMVVPLSASHAHSLANLRKTPDEV 154

Query: 127 LERARQVASRAASAGLS--VRGYVSCIFADPYDGPTRPSSVLRCTKALLDAGCYEVSLGD 184
           +    ++ +   ++G S  + G V   F     G    S VLR  +ALLDAG   VSL D
Sbjct: 155 VAEVARIRALRDASGRSTLIEGGVGTAFGCTLQGEVAESEVLRLMQALLDAGADHVSLAD 214

Query: 185 TLGIGTPADVRWLITYLQDNGVPLEMLAGHFHDTYGGAVANVWEAYKCGLRMFDSSVAGL 244
           T+G   PA V  L    +   V   +   HFHDT G  +ANV+ A++ G+  FD+ +AG+
Sbjct: 215 TVGFADPASVARLFDKARAL-VGDRLACAHFHDTRGMGLANVYAAWQTGITRFDACLAGI 273

Query: 245 GGCPXALGAKGNVASEDLVYMFERSGIHTGVDLSKLVETGEWISRQLSIAISSRAGAALW 304
           GGCP A GA GNV +EDLV+M ER G+ TG+D+S L+   + ++  L       AG  L 
Sbjct: 274 GGCPHAPGASGNVTTEDLVFMLERMGVATGIDVSALLALRQRVAGWL-------AGETLH 326

Query: 305 AMRKQTAVPKS 315
               Q  +P++
Sbjct: 327 GTLWQAGLPQN 337


Lambda     K      H
   0.318    0.134    0.389 

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: 430
Number of extensions: 21
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 599
Length of database: 349
Length adjustment: 33
Effective length of query: 566
Effective length of database: 316
Effective search space:   178856
Effective search space used:   178856
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 (21.7 bits)
S2: 51 (24.3 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