GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Novosphingobium barchaimii LL02

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate WP_059153425.1 V474_RS21830 iron ABC transporter permease

Query= SwissProt::P15030
         (332 letters)



>NCBI__GCF_001046635.1:WP_059153425.1
          Length = 331

 Score =  155 bits (391), Expect = 2e-42
 Identities = 109/334 (32%), Positives = 174/334 (52%), Gaps = 9/334 (2%)

Query: 1   MTAIKHPVLLWGLPVAALIIIFWLSLFCYSAIPVSGADATRALLPGHTPTLPEALVQNLR 60
           M++ +HP L+  L   A +++  L+      +P+S A    A   GH   + +A++  LR
Sbjct: 1   MSSQRHPALIPLL--LAGVLVMGLASVNLGPVPLSPARILAAFT-GHGDEIAQAILFQLR 57

Query: 61  LPRSLVAVLIGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALSPTPIAGYS 120
           LPR+LVA+L+GA+L L G +LQ    NP+A PS+LG ++ +AL                 
Sbjct: 58  LPRTLVALLVGATLGLTGAVLQGYLRNPLAEPSVLGASNASALGAVAAIYFGVADWHPAL 117

Query: 121 LSFIAACGGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDH--A 178
           L  ++   G ++ +L+    G    +     LILAGIA+S        + L L+ +   A
Sbjct: 118 LPLLSIASGLIALMLLFALAG---RSESPLTLILAGIAVSTLAGAGISLALNLSPNPFAA 174

Query: 179 YGIFYWLAGGVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRL 238
             I  WL G + +   + VW  LP V+  + ++L     L+ L+L +  A +LGV+L+R 
Sbjct: 175 MEIMAWLLGSIENRTMEHVWIALPCVMLGMALLLYDPRALDALSLGEDGARSLGVDLSRT 234

Query: 239 RLVINMLVLLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLAD 298
           R+ + + V + VG  V+V+G + F+GL+VPHL R         +L  S+L GA L+  AD
Sbjct: 235 RIRLLLGVAIGVGGAVAVSGSIGFVGLIVPHLIRPLTDRSPSALLLPSLLGGAILLTGAD 294

Query: 299 VLARALAFPGDLPAGAVLALIGSPCF-VWLVRRR 331
           +L R +    +L  G V A +G P F V L+R R
Sbjct: 295 ILVRLIPTASELKLGVVTAFLGVPVFLVHLLRER 328


Lambda     K      H
   0.327    0.140    0.436 

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: 319
Number of extensions: 17
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: 332
Length of database: 331
Length adjustment: 28
Effective length of query: 304
Effective length of database: 303
Effective search space:    92112
Effective search space used:    92112
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 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