GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Stenotrophomonas chelatiphaga DSM 21508

Align 2-methylcitrate synthase; 2-MCS; MCS; Citrate synthase; EC 2.3.3.5; EC 2.3.3.16 (characterized)
to candidate WP_057687496.1 ABB28_RS16700 citrate synthase

Query= SwissProt::O34002
         (379 letters)



>NCBI__GCF_001431535.1:WP_057687496.1
          Length = 425

 Score =  200 bits (508), Expect = 7e-56
 Identities = 133/392 (33%), Positives = 204/392 (52%), Gaps = 33/392 (8%)

Query: 5   TIHKGLAGVTADVTAISKVNSDTNSLLYRGYPVQELAAKCSFEQVAYLLWNSELPNDSEL 64
           T   G     +  +AI+ ++ D   LLYRGYP+++L+ K S+ +V YLL N E P+ ++L
Sbjct: 43  TYDSGFTATASCKSAITYIDGDKGVLLYRGYPIEQLSEKSSYVEVVYLLINGERPDAAQL 102

Query: 65  KAFVNFERSHRKLDENVKGAIDLLSTACHPMDVARTAVSVL-GANHARAQDSSPEANLEK 123
           KAF     +   +D +V   I   +   HPM +   A++ L G  HA    S  E   + 
Sbjct: 103 KAFNEELAAEATVDASVNTLIGSFAKDAHPMAILTAAIAQLSGIYHASLDLSDAEQRRKA 162

Query: 124 AMSLLATFPSVVAYDQRRRRGEELIEPREDLDYSANFLWMTFGE-----EAAPEVVEAFN 178
           A+ L+A  P++ A   R  +G     P   LDY + FL  TF       E   +VV+A +
Sbjct: 163 AVRLIAKVPTLSALIYRHGKGLPANTPDTSLDYVSRFLKQTFESADGQYELNQDVVKALD 222

Query: 179 VSMILYAEHSFNASTFTARVITSTLADLHSAVTGAIGALKGPLHGGANEAVMHTFEEIGI 238
           +  IL+A+H  NAST T R++ ST A+ +++V   + AL GP HGGANEAV+   EEIG 
Sbjct: 223 LLFILHADHEQNASTSTVRMVGSTGANPYASVAAGVTALWGPAHGGANEAVLKMLEEIG- 281

Query: 239 RKDESLDEAATRSKAWMVDALAQKKKVMGFGHRVYKNGDSRVPTMKSALDAMIKHYDRPE 298
              ++++ A  ++K           ++MGFGHRVYKN D R   +      ++      E
Sbjct: 282 -SADNVESAVVKAK-----DKTSGFRLMGFGHRVYKNFDPRAKVIGVMTGKVL------E 329

Query: 299 MLGLYNGL--------EAAMEE----AKQIKPNLDYPAGPTYNLMGFDTEMFTPLFIAAR 346
            LG+ + L        +AA+++    A+++ PN+D+ +G  Y  +   TEMFT +F   R
Sbjct: 330 QLGVQDPLLDVAVKLEQAALQDDYFVARKLYPNVDFYSGIIYKALQIPTEMFTVMFALGR 389

Query: 347 ITGWTAHIMEQVADNALI--RPLSEYNGPEQR 376
            +GW AH +EQ  D  +   RP   Y G + R
Sbjct: 390 TSGWVAHWLEQQVDPEMKIGRPRQVYTGSDVR 421


Lambda     K      H
   0.316    0.130    0.376 

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: 378
Number of extensions: 17
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: 379
Length of database: 425
Length adjustment: 31
Effective length of query: 348
Effective length of database: 394
Effective search space:   137112
Effective search space used:   137112
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 (21.6 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