Align α,α-trehalase / α-glucosidase (TTC0107) (EC 3.2.1.20|3.2.1.28) (characterized)
to candidate WP_078429218.1 BK574_RS15505 alpha-glucosidase
Query= CAZy::AAS80455.1 (528 letters) >NCBI__GCF_002019605.1:WP_078429218.1 Length = 555 Score = 360 bits (925), Expect = e-104 Identities = 199/505 (39%), Positives = 287/505 (56%), Gaps = 44/505 (8%) Query: 2 WWKEAVIYQVYPRSFQDTNGDGVGDLEGVRRRLPYLKSLGVDALWLSPFYKSPMKDFGYD 61 WWKE+V+YQ+YPRSF+D+NGDG+GDL+G+ +L YLK LG+D +WLSP Y SP D GYD Sbjct: 5 WWKESVVYQIYPRSFKDSNGDGIGDLQGIISKLDYLKELGIDVIWLSPVYSSPNDDNGYD 64 Query: 62 VADYCDVDPVFGTLQDFDRLLEEAHALGLKVLVDLVPNHTSSEHPWFLESRASRNSPKRD 121 ++DY D+ FGT+ D+++LL+E H +K+++DLV NH+S EHPWF+ES +S+ + RD Sbjct: 65 ISDYQDIMGEFGTMADWEQLLKEVHNREMKLIMDLVVNHSSDEHPWFIESSSSKTNKYRD 124 Query: 122 WYIWKDPAPDGGPPNNWQSFFGGPAWTLDEATGQYYLHQFLPEQPDLNWRNPEVREAIYE 181 +YIW+ PA +G PNNW S FGG AW DE T +YYLH F +QPDLNW P++RE IY+ Sbjct: 125 YYIWR-PAKEGKEPNNWGSNFGGSAWQYDEQTDEYYLHLFSKKQPDLNWETPDLREDIYK 183 Query: 182 VMRFWLRRGVDGFRVDVLWLLAEDLLFRDEPGNPDWRPGMWDRGRHLHIFTEDQPETYAY 241 +M +WL +G+DGFR+DV+ +++ D+ P + + + + P+ + Y Sbjct: 184 MMTWWLEKGIDGFRMDVINFISKVEGLPDDEVKPGKKYASGSK------YYRNGPKIHKY 237 Query: 242 VREMRQ-VLDEFSEPGRERVMVGEIYLPYPQLVRYYQAGCHLPFNFHLIFR--------- 291 ++EM Q VL ++ + VGE+ P L + Y A N F Sbjct: 238 LQEMNQKVLSNYNV-----MTVGEMPGVSPDLAKLYTAEARDELNMVFQFEHMGLDNGPN 292 Query: 292 ---GLPDWRPENLARIVEEYESLLTRWDWPNWVLGNHDQPRLASRLG------EAQARVA 342 L + ++L + +++ L R W + NHDQPR SR G A A + Sbjct: 293 GKWDLKELELQDLKNNLSKWQIELEREGWNSLYFNNHDQPRSVSRFGHDGEYHRASATML 352 Query: 343 AMLLFTLRGTPTWYYGDEIGMKNGEIPP-EKVQDPAALRQKDRLGEHNL----------P 391 A LL ++GTP Y G+E GM N E +D L + E + Sbjct: 353 ATLLHMMKGTPYVYQGEEFGMTNVAFSSIEDYRDIETLNFYNEEKEQGVAEELIMASIHA 412 Query: 392 PGRDPERTPMQWDDTPFAGFSTVEPWLPVNPDYKTRNVAAQEQDPRSMLHLVRRLIALRK 451 RD RTP+QWDD AGF+T +PW+ VNP+Y N +DP S+ H ++LI LRK Sbjct: 413 KSRDNARTPVQWDDHLNAGFTTGKPWINVNPNYMKINAKRALEDPMSIFHYYKKLIQLRK 472 Query: 452 DPD-LLYGAYR-TYRAREGVYAYLR 474 D ++YG+Y+ V+AY R Sbjct: 473 TYDVIVYGSYQLLLEDHPTVFAYQR 497 Lambda K H 0.321 0.141 0.466 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: 995 Number of extensions: 49 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 528 Length of database: 555 Length adjustment: 35 Effective length of query: 493 Effective length of database: 520 Effective search space: 256360 Effective search space used: 256360 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
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:
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