GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ligJ in Cupriavidus basilensis 4G11

Align 2-keto-4-carboxy-3-hexenedioate hydratase; KCH hydratase; EC 4.2.1.- (characterized)
to candidate RR42_RS28355 RR42_RS28355 amidohydrolase

Query= SwissProt::G2IQQ5
         (341 letters)



>FitnessBrowser__Cup4G11:RR42_RS28355
          Length = 334

 Score =  221 bits (563), Expect = 2e-62
 Identities = 129/340 (37%), Positives = 187/340 (55%), Gaps = 11/340 (3%)

Query: 3   MIIDCHGHYTVLPKAHDEWREQQKAAFKAGQPAPPY-PEISDDEIRETIEANQLRLIKER 61
           MIID H H  + P++      +  A    G+  P   P++ D  +R+  E   ++ + + 
Sbjct: 1   MIIDSHAHIVMPPESF-----RYMAELVGGRANPSTTPKVPDASVRKVAE-ELVQSMDKV 54

Query: 62  GADMTIFSPRASAMAPHVGDQSVAVPWAQACNNLIARVVDLFPETFAGVCMLPQ-SPEAD 120
           G D+   SPR       V    V   W++ CN+LIAR V LFP+ F GV  LPQ   E+ 
Sbjct: 55  GTDVQFISPRPYLQMHSVKPGRVTELWSRHCNDLIARFVALFPDRFRGVAGLPQYMNESP 114

Query: 121 MTSSIAELERCVNELGFIGCNLNPDPGGGHFKHPP-LTDRFWYPFYEKMVELDVPAMIHV 179
              ++ ELERCV ELGF+GC +NPDP  G    PP L D FWYP Y+ M +LDVP +IH 
Sbjct: 115 ALRAVPELERCVKELGFVGCLINPDPTEGEGPTPPGLGDPFWYPLYDAMTQLDVPGLIHS 174

Query: 180 SGSCNPAMHATGAYYLAADTIAFMQLLQGNLFADFPTLRFIIPHGGGAVPYHWGRFRGLA 239
           +GSC+ A  +    ++  ++IA + LL   +F  +P L+ ++ HGGGA+PY  GRFR  +
Sbjct: 175 AGSCS-ARESYTLKFINEESIAIVSLLGSKVFDTYPGLKIVVAHGGGAIPYQMGRFRSWS 233

Query: 240 DMLKQPSLDTLLMNNVFFDTCVYHQPGINLLADVIDNKNILFGSEMVGAVRGIDPTTGHY 299
               +       +  ++FDTC Y +  I LL  V    N+LFG+E  G     DP +G  
Sbjct: 234 VRKGETVSFDEQLKRLYFDTCNYSKEAIELLLKVAGTDNVLFGTEKPGTGSARDPVSGRD 293

Query: 300 FDDTKRYIDALD-ISDQERHAIFEGNTRRVFPRLDAKLKA 338
           +DD K  I+++D +S+Q+R  IFE N  RV+ R   K +A
Sbjct: 294 YDDMKPVIESIDWLSEQQRRNIFECNCTRVYSRAFRKDEA 333


Lambda     K      H
   0.323    0.140    0.442 

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: 337
Number of extensions: 20
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: 341
Length of database: 334
Length adjustment: 28
Effective length of query: 313
Effective length of database: 306
Effective search space:    95778
Effective search space used:    95778
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 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