GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_2562 in Cupriavidus basilensis 4G11

Align ABC transporter for L-Histidine, periplasmic substrate-binding component 2 (characterized)
to candidate RR42_RS16940 RR42_RS16940 ABC transporter permease

Query= reanno::acidovorax_3H11:Ac3H11_2562
         (321 letters)



>FitnessBrowser__Cup4G11:RR42_RS16940
          Length = 323

 Score =  492 bits (1267), Expect = e-144
 Identities = 245/315 (77%), Positives = 276/315 (87%), Gaps = 4/315 (1%)

Query: 10  SLAAAAACVMAL---AAPAQAQDTKIVLGMSGWTGFAPLTLADKAGIFKKNGLDVEIKMI 66
           SLA A A V+A    A  AQAQ T++ LGMSGWTGFAPLTLADKAGIFKK+G+DV+IKMI
Sbjct: 10  SLAVAVAAVVATLGAAGTAQAQATQVTLGMSGWTGFAPLTLADKAGIFKKHGVDVDIKMI 69

Query: 67  PQKDRHLALASKSIQCAATTVETHVAWNANGVPIVQIFQMDKSYGADGIAVRGDIKSFAD 126
           PQKDRHLALA+ +IQCAATTVETHVAWNANGVPI QI Q+DKSYGADG+AVRGD+K FAD
Sbjct: 70  PQKDRHLALAAGAIQCAATTVETHVAWNANGVPITQIVQLDKSYGADGLAVRGDVKGFAD 129

Query: 127 LKGKTIGVDAPGTAPYFGLAWMLSKNGMSLKDVKTTTLSPQAAAQAFVAGQNDAAMTYEP 186
           LKGKTIGVDAPGTAPYFGLAWML KNGMSLKDVKTTTLSPQAAAQAFVAGQNDAAMTYEP
Sbjct: 130 LKGKTIGVDAPGTAPYFGLAWMLKKNGMSLKDVKTTTLSPQAAAQAFVAGQNDAAMTYEP 189

Query: 187 YLSTVRDNPAAGKILATTLDYPMVMDTVGCDPTWLKANGKAAQALANSYFQALDMIKADP 246
           YLS+VR NP  GKILATTLDYPMVMDT+GC P WLK N KAAQAL +SYF+ALDMI+ DP
Sbjct: 190 YLSSVRQNPDKGKILATTLDYPMVMDTLGCAPKWLKDNPKAAQALVDSYFEALDMIRQDP 249

Query: 247 AKSNEIMGAAVKQTGEQFAKSSSFLRWQDKAANQKFFAGELTTFMKDATAILLEAGIIRK 306
           AK+N++MGAAVKQ+GEQFAKSS++LRWQD+ AN+KFF GEL +F K+A  +LLE G+IR+
Sbjct: 250 AKANDVMGAAVKQSGEQFAKSSAYLRWQDRDANRKFFGGELASFSKEAAQVLLEIGVIRQ 309

Query: 307 ANEDLAVTFDASFIK 321
              D+   +DA FIK
Sbjct: 310 V-PDVTALYDARFIK 323


Lambda     K      H
   0.317    0.129    0.374 

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: 425
Number of extensions: 8
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: 321
Length of database: 323
Length adjustment: 28
Effective length of query: 293
Effective length of database: 295
Effective search space:    86435
Effective search space used:    86435
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 17 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