Aligments for a candidate for liuD in Pseudomonas fluorescens GW456-L13

GapMind for catabolism of small carbon sources

Aligments for a candidate for liuD in Pseudomonas fluorescens GW456-L13

Align methylcrotonoyl-CoA carboxylase (EC 6.4.1.4) (characterized)
to candidate PfGW456L13_2287 Geranyl-CoA carboxylase carboxyl transferase subunit

Query= BRENDA::Q9I297
         (535 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2287
          Length = 538

 Score =  461 bits (1186), Expect = e-134
 Identities = 248/541 (45%), Positives = 336/541 (62%), Gaps = 11/541 (2%)

Query: 1   MAILHTQINPRSAEFAANAATMLEQVNALRTLLGRIHEGGGSAAQARHSARGKLLVRERI 60
           M ++ +Q++P S  FA N A ML  +  +R L   +      A + +   RG+LL RER+
Sbjct: 1   MPVIQSQLDPHSESFAQNRAAMLSAIEQVRVLEQNLLNKAAEA-RPKFEKRGQLLPRERL 59

Query: 61  NRLLDPGSPFLELSALAAHEVYGEE---VAAAGIVAGIGRVEGVECMIVGNDATVKGGTY 117
           N LLDPG+PFLEL++LA ++++ ++    A  G++AGIG V GV  ++V N++ ++GGT 
Sbjct: 60  NLLLDPGAPFLELASLAGYKLHDDKDGSSAGGGLIAGIGYVSGVRVLVVANNSAIRGGTI 119

Query: 118 YPLTVKKHLRAQAIALENRLPCIYLVDSGGANLPRQDEVFPDREHFGRIFFNQANMSARG 177
            P  +KK LR Q IA+EN+LP I L +SGGANL    E+F +     R F NQA MSA G
Sbjct: 120 SPSGLKKSLRLQQIAMENKLPVITLAESGGANLNYAAEIFVEG---ARSFANQARMSAMG 176

Query: 178 IPQIAVVMGSCTAGGAYVPAMSDETVMVREQATIFLAGPPLVKAATGEVVSAEELGGADV 237
           +PQ+ VV GS TAGGAY P +SD  V+VR +A +FLAGPPL+KAATGEV + EELGGA++
Sbjct: 177 LPQVTVVHGSATAGGAYQPGLSDYVVVVRGKAKLFLAGPPLLKAATGEVATDEELGGAEM 236

Query: 238 HCKVSGVADHYAEDDDHALAIARRCVANLNWRKQ-GQLQCRAPRAPLYPAEELYGVIPAD 296
           H + +G A++ AE+D   +   R  ++ L W +Q   L  R    PLYP +EL G+IP D
Sbjct: 237 HAQTAGTAEYLAENDADGVRQVREIISLLPWNEQLPPLPERRWEEPLYPIDELLGLIPDD 296

Query: 297 SKQPYDVREVIARLVDGSEFDEFKALFGTTLVCGFAHLHGYPIAILANNGILFAEAAQKG 356
            K+PYD RE+IARL D S F EFK  F    +CG   + G     + NNG +  + A K 
Sbjct: 297 PKKPYDAREIIARLADASNFLEFKGEFDQQTLCGHLKIQGRACGFIGNNGPITPKGASKA 356

Query: 357 AHFIELACQRGIPLLFLQNITGFMVGQKYEAGGIAKHGAKLVTAVACARVPKFTVLIGGS 416
           A FI+L  Q   PLLF  N TGFMVG + E  G+ KHGAK++ AVA ARVPK T+++GGS
Sbjct: 357 AQFIQLCDQSQTPLLFFHNTTGFMVGTESEQQGVIKHGAKMIQAVANARVPKLTIVVGGS 416

Query: 417 FGAGNYGMCGRAYDPRFLWMWPNARIGVMGGEQAAGVLAQVKREQAERAGQQLGVEEEAK 476
           +GAGNY MCGR  DPRF++ WPN+R  VMGG QA  VL  V   +  + G     +    
Sbjct: 417 YGAGNYAMCGRGLDPRFIFAWPNSRTAVMGGAQAGKVLRIVTEAKQAKDGLVPDPKMLDM 476

Query: 477 IKAPILEQYEHQGHPYYSSARLWDDGVIDPAQTREVLALALSAALNA---PIEPTAFGVF 533
           ++    ++ + Q    Y SA LWDDG+IDP  TR +L   L     A   P++  +FGV 
Sbjct: 477 LEQVTAQKLDSQSTALYGSANLWDDGLIDPRDTRTLLGYLLDICHEAEVRPLQANSFGVA 536

Query: 534 R 534
           R
Sbjct: 537 R 537


Lambda     K      H
   0.321    0.137    0.409 

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: 764
Number of extensions: 35
Number of successful extensions: 5
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: 535
Length of database: 538
Length adjustment: 35
Effective length of query: 500
Effective length of database: 503
Effective search space:   251500
Effective search space used:   251500
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: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources