GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Thiohalomonas denitrificans HLD2

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate WP_092996195.1 BLP65_RS09975 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::Smeli:SM_b21216
         (360 letters)



>NCBI__GCF_900102855.1:WP_092996195.1
          Length = 338

 Score =  298 bits (762), Expect = 2e-85
 Identities = 169/359 (47%), Positives = 225/359 (62%), Gaps = 23/359 (6%)

Query: 1   MSALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60
           M+++++ N+ KR+G  E +KGID+ +E+G   V +G SGCGKSTLL +IAGL E + G I
Sbjct: 1   MASVDLENVTKRFGRTEVIKGIDLTIENGRLTVFVGPSGCGKSTLLRLIAGLEEVTSGKI 60

Query: 61  LIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARL 120
            IG+ +V    P +R +AMVFQSYALYP++ V  N+ FGL++ R  + E ++ VR  AR+
Sbjct: 61  HIGDENVTDWPPAERGVAMVFQSYALYPHMKVFDNMAFGLKISRTKRNEIEERVRHAARI 120

Query: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180
           L+IE LL+ KP +LSGGQRQRVAIGRA+VR P+VFLFDEPLSNLDA LR++MR EL  L 
Sbjct: 121 LRIEPLLNHKPGELSGGQRQRVAIGRAIVREPKVFLFDEPLSNLDASLRVQMRLELASLQ 180

Query: 181 QMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMN 240
           + L  T+VYVTHDQ EAMTL   I V+ +GR+EQ+  P EVY  PA  +VAGF+GSP MN
Sbjct: 181 RELDATMVYVTHDQTEAMTLGHTIVVLNEGRVEQVGTPLEVYRNPANRFVAGFIGSPEMN 240

Query: 241 ILDAEMTANGLKIEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAGSEAQRLTASV 300
            L+             EE LP+P      A     V +GIRPE + L  G     L   +
Sbjct: 241 FLE------------LEEKLPIPKPPLPEA-----VTLGIRPEHVILGDGP----LQGKI 279

Query: 301 EVVELTGPE-LVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESGRSLR 358
            +VE  G E  +     G +R+TA      +   G   A  F    LH FD + GR+++
Sbjct: 280 TLVERLGSESFLHLELPGEERVTARASGDLSARPGDTMAMEFPSEHLHFFD-DDGRTIQ 337


Lambda     K      H
   0.320    0.136    0.385 

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: 346
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: 360
Length of database: 338
Length adjustment: 29
Effective length of query: 331
Effective length of database: 309
Effective search space:   102279
Effective search space used:   102279
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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