GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Paenisporosarcina indica PN2

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate WP_075619375.1 GY23_RS11545 iron ABC transporter permease

Query= SwissProt::P15030
         (332 letters)



>NCBI__GCF_001939075.1:WP_075619375.1
          Length = 332

 Score =  192 bits (487), Expect = 1e-53
 Identities = 108/323 (33%), Positives = 183/323 (56%), Gaps = 5/323 (1%)

Query: 11  WGLPVAALIIIFWLSL-FCYSAIPVSGADATRALLPGHTPTLPEALVQNLRLPRSLVAVL 69
           WG+ +   +I+  +S    Y     +  DA  AL    T      +++++RLPR+L+A  
Sbjct: 10  WGIVIGTTLILLLMSASLVYGYTNTTWIDAYLALFDPTTSN-KHLIIRDVRLPRALIAAF 68

Query: 70  IGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSA-LSPTPIAGYSLSFIAACG 128
           +GA L ++G ++Q++T NP++SPS+LGIN+GA+  + +    LS   +  Y   +++  G
Sbjct: 69  VGACLGVSGAIMQSITRNPLSSPSILGINAGASFFVVVGVVFLSVQSLQSYM--WLSFAG 126

Query: 129 GGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDHAYGIFYWLAGG 188
              ++LLV       R      KL LAG A++A     T+  L+L E     + +WLAG 
Sbjct: 127 ATFAFLLVFILSSTGREGLTPLKLTLAGSAITALFTSFTQGLLVLNETALDQVLFWLAGS 186

Query: 189 VSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLVINMLVLL 248
           V++   + ++  LP ++ A+ +V   A +LN+L++ D  A  LG     ++       ++
Sbjct: 187 VANRPLELLFHALPYIIVALLIVFFRAKELNVLSIGDDVAVGLGQRTAWIKFTFGTCAVV 246

Query: 249 LVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLARALAFPG 308
           L G+ V+VAGP+ F+G+++PHL R   G D R +LP S L GA L+L+AD+ +R +  P 
Sbjct: 247 LAGSAVAVAGPIGFVGIIIPHLIRSLVGLDHRWILPYSALGGAALLLIADIGSRYVLMPQ 306

Query: 309 DLPAGAVLALIGSPCFVWLVRRR 331
           +LP G + ALIG P F+++ RR+
Sbjct: 307 ELPVGVMTALIGVPFFIFVARRK 329


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: 297
Number of extensions: 13
Number of successful extensions: 3
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: 332
Length adjustment: 28
Effective length of query: 304
Effective length of database: 304
Effective search space:    92416
Effective search space used:    92416
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.

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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