GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citE in Desulfitobacterium hafniense DCB-2

Align Citrate lyase subunit beta; Citrase beta chain; Citrate (pro-3S)-lyase subunit beta; Citryl-CoA lyase subunit; EC 4.1.3.6; EC 4.1.3.34 (characterized)
to candidate WP_005812973.1 DHAF_RS15385 CoA ester lyase

Query= SwissProt::P0A9I1
         (302 letters)



>NCBI__GCF_000021925.1:WP_005812973.1
          Length = 295

 Score =  165 bits (418), Expect = 1e-45
 Identities = 103/284 (36%), Positives = 159/284 (55%), Gaps = 2/284 (0%)

Query: 15  RSMLFVPGANAAMVSNSFIYPADALMFDLEDSVALREKDTARRMVYHALQHPLYRDIETI 74
           RS++++PG N  MV+ +   PAD + FDLED+V   EK+TAR++V   L++      +  
Sbjct: 5   RSVMYIPGNNPKMVAKAPEIPADIITFDLEDAVPPAEKETARQIVRENLEYGAKGGAQVF 64

Query: 75  VRVNALDSEWGVNDLEAVVRGGADVVRLPKTDTAQDVLDIEKEILRIEKACGREPGSTGL 134
           VR+N  ++    +DLEA+V  G + V L KT  A DV  +E ++  +E   G   G+  +
Sbjct: 65  VRINNWETGLTNDDLEAIVWPGLNGVTLAKTGCAADVQRLEWKLEELEMRRGIPVGTVKI 124

Query: 135 LAAIESPLGITRAVEIAHASERLIGIALGAEDYVRNLRTERSPEGTELLFARCSILQAAR 194
              +E+  GI  A E   AS+R +    GA DY R++R + + E  E  + R  +  A R
Sbjct: 125 SMLLETAKGIAHAEECCLASKRNVNAIFGAVDYCRDMRVKITNEAVEQQYGRAKVGVACR 184

Query: 195 SAGIQAFDTVYSDANNEAGFLQEAAHIKQLGFDGKSLINPRQIDLLHNLYAPTQKEVDHA 254
           +AGI A D  + D  N   F +  A  KQ+G++G+ +I+P Q++  + +YAP   +V  A
Sbjct: 185 AAGIVAIDAPFVDYANIPAFEKNVAEGKQMGYEGRMIIHPGQVEPSNRMYAPDPADVKWA 244

Query: 255 RRVVEA-AEAAAREGLGVVSLNGKMVDGPVIDRARLVL-SRAEL 296
             VV+   E    +G   VSLNGKMVD PV   A+ +L S+AE+
Sbjct: 245 NDVVKVFEEEGLAKGKAAVSLNGKMVDTPVYLNAKDILASQAEI 288


Lambda     K      H
   0.318    0.134    0.369 

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: 197
Number of extensions: 9
Number of successful extensions: 2
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: 302
Length of database: 295
Length adjustment: 27
Effective length of query: 275
Effective length of database: 268
Effective search space:    73700
Effective search space used:    73700
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: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

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:

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