GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Pseudomonas putida KT2440

Align 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate PP_1412 PP_1412 3-hydroxyisobutyryl-CoA hydrolase

Query= reanno::pseudo1_N1B4:Pf1N1B4_4790
         (356 letters)



>FitnessBrowser__Putida:PP_1412
          Length = 368

 Score =  245 bits (625), Expect = 2e-69
 Identities = 151/350 (43%), Positives = 194/350 (55%), Gaps = 9/350 (2%)

Query: 7   EVLAEVRN-HIGHLTLNRPAGLNAITLDMVRSLQQQLDAWAQDPQVHAVVLRGAGEKAFC 65
           EVL  V    IG  TL+ P  LNA+ L M+  L +QL AWA+DP +  V+LRG G KAFC
Sbjct: 6   EVLTGVDGARIGIATLDAPKALNALNLPMIEVLGEQLHAWARDPGIVCVLLRGNGAKAFC 65

Query: 66  AGGDIRSLYDSFK----SGDTLHEDFFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLV 121
           AGGD+R+L  + +    S   L   FF  EY LD A+H Y KP+L    G VLGGGMGL+
Sbjct: 66  AGGDVRALAQACRDHPGSVPPLAASFFAAEYRLDFALHTYPKPLLCWGHGHVLGGGMGLL 125

Query: 122 QGADLRVVTERSRLAMPEVAIGYFPDVGGSHFLPRVPGELGIYLGVSGVQIRAADALYCG 181
           QGA++R+VT  SRLAMPE++IG +PDVG S FL R+PG+LG++ G++G  I A DAL  G
Sbjct: 126 QGANVRIVTPSSRLAMPEISIGLYPDVGASWFLARLPGKLGLFFGLTGAPINARDALDLG 185

Query: 182 LADWYLESNKLGTLDEQLDQLQWHETPLKDLQGLL---AKLAVQQLPAAPLAALRPAIDH 238
           LAD +L  ++   L E+L QL W E     L  LL      A  +LP A     R  ID 
Sbjct: 186 LADRFLGEHQQEALIEELLQLNWQEQTAIQLNSLLKAEQHRACAELPDAQWLPRRHEIDQ 245

Query: 239 FFALPDVPSMVEQLRAVTVADSHEWATATADLLESRSPLAMGVTLEMLRRGRHLSLEQCF 298
              + D  S    L  +   D    A A   L E   PL   +  E +RR R+LSL Q F
Sbjct: 246 LLDVADAASAWRALERLKQHDDPLLADAGHRLHEG-CPLTAHLVWEQIRRARYLSLAQVF 304

Query: 299 ALELHLDRQWFERGDLIEGVRALLIDKDKNPRWSPPTLQALDAGHVASFF 348
            +E  +        +  EGVRA L+DKD  PRW  P +  +    V + F
Sbjct: 305 QMEYSMSLNCCRHPEFSEGVRARLLDKDNQPRWHWPDVAQVPTAVVEAHF 354


Lambda     K      H
   0.322    0.138    0.422 

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: 411
Number of extensions: 21
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: 356
Length of database: 368
Length adjustment: 29
Effective length of query: 327
Effective length of database: 339
Effective search space:   110853
Effective search space used:   110853
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 (21.9 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