GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Thioalkalivibrio thiocyanodenitrificans ARhD 1

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_018231851.1 THITHI_RS0104340 2-methylcitrate synthase

Query= BRENDA::Q2Z1A8
         (398 letters)



>NCBI__GCF_000378965.1:WP_018231851.1
          Length = 385

 Score =  611 bits (1576), Expect = e-179
 Identities = 286/382 (74%), Positives = 334/382 (87%)

Query: 16  TASEPAAPRVKKSVALSGVTAGNTALCTVGRTGNDLHYRGYDILDIAETCEFEEIAHLLV 75
           T +    PR KKSVALSG  AGNTA+CTVGRTGNDLHYRGYDILD A+  EFEEIAHLL+
Sbjct: 4   TDTTQTKPRPKKSVALSGTVAGNTAICTVGRTGNDLHYRGYDILDFADKAEFEEIAHLLI 63

Query: 76  HGKLPTKSELAAYKAKLKSLRGLPANVKAALEWVPASAHPMDVMRTGVSVLGTVLPEKED 135
           HG LP ++ELAAYK +L++LRGLPA ++  LE +P SAHPMDVMRT VS+LGT+ PEKED
Sbjct: 64  HGTLPDRAELAAYKERLRALRGLPAALRTVLEQIPPSAHPMDVMRTAVSMLGTLEPEKED 123

Query: 136 HNTPGARDIADRLMASLGSMLLYWYHYSHNGRRIEVETDDDSIGGHFLHLLHGEKPSALW 195
               GAR I DRL+ASLGS LLYWYH++HNGRRI+VETDDDS+GGHFLHL+HG  PS  W
Sbjct: 124 MTVAGARQIGDRLLASLGSALLYWYHFAHNGRRIDVETDDDSLGGHFLHLMHGRAPSEPW 183

Query: 196 ERAMHTSLNLYAEHEFNASTFTARVIAGTGSDMYSSISGAIGALRGPKHGGANEVAFEIQ 255
            RAMHTSLNLYAEHEFNASTFT+RV+AGT +D+YS+I+GAIGALRGPKHGGANEVA +IQ
Sbjct: 184 VRAMHTSLNLYAEHEFNASTFTSRVVAGTNADLYSAITGAIGALRGPKHGGANEVACDIQ 243

Query: 256 KRYDNPDEAQADITRRVGNKEVVIGFGHPVYTTGDPRNQVIKEVAKKLSKDAGSMKMFDI 315
            RYD+PD+A+ADI  RVG KE++IGFGHPVYTTGDPRN+VIK VAK+LS+D  +M MF +
Sbjct: 244 LRYDDPDQAEADIRERVGRKEIIIGFGHPVYTTGDPRNEVIKAVAKRLSEDRHTMTMFAV 303

Query: 316 AERLETVMWDIKKMFPNLDWFSAVSYHMMGVPTAMFTPLFVIARTSGWAAHIIEQRIDNK 375
           A+RLE+VMWD+KKMFPNLDWFSAVSYHMMG+PTA+FTP+FVI+RT+GW AH+IEQR+D K
Sbjct: 304 ADRLESVMWDLKKMFPNLDWFSAVSYHMMGIPTALFTPIFVISRTTGWVAHVIEQRLDGK 363

Query: 376 IIRPSANYTGPENLKFVPIGKR 397
           IIRPSANYTGPEN K+VPI KR
Sbjct: 364 IIRPSANYTGPENRKWVPIDKR 385


Lambda     K      H
   0.317    0.133    0.396 

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: 555
Number of extensions: 15
Number of successful extensions: 1
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: 398
Length of database: 385
Length adjustment: 31
Effective length of query: 367
Effective length of database: 354
Effective search space:   129918
Effective search space used:   129918
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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