Align Rhamnulokinase (EC 2.7.1.5) (characterized)
to candidate CA265_RS02640 CA265_RS02640 carbohydrate kinase
Query= reanno::Cola:Echvi_1574 (448 letters) >lcl|FitnessBrowser__Pedo557:CA265_RS02640 CA265_RS02640 carbohydrate kinase Length = 461 Score = 395 bits (1015), Expect = e-114 Identities = 207/439 (47%), Positives = 280/439 (63%), Gaps = 8/439 (1%) Query: 3 PIPVIAIFDIGKTNKKFFLFDEHSNEIKQEYNKIPLTEDEDGFECDDLVALSEWITSTVE 62 P PVIAIFD+GKTNKK FL DE+ + + + + T DEDG C++L +L + ++ Sbjct: 2 PKPVIAIFDVGKTNKKLFLIDENYSIVYERSARFVETVDEDGEPCENLESLRSSVYDSLH 61 Query: 63 EICQSPDYALKGINFSTYGASFVHIDADGNPLTPLYNYLKEIPQEIIDEFYRQYP-EETN 121 ++ Q ++ ++ INFSTYGASFV++D +GNPLTPLYNYLKE P+ + FY +Y EE Sbjct: 62 QVLQLKEFDVRAINFSTYGASFVYLDENGNPLTPLYNYLKEYPEALKKAFYAEYGGEEKI 121 Query: 122 NLETASPSLGMLNSGLQLYWLKKTKPDLFSKIAYSLHFPQYLSYLFTKKAVSEPTSIGCH 181 +LETASP LG LNSG+QLY LK KP++F K+ ++LH PQYLSYL T KAV++ TSIGCH Sbjct: 122 SLETASPILGSLNSGMQLYRLKNEKPEIFKKVKWALHLPQYLSYLITGKAVADITSIGCH 181 Query: 182 TRLWDFQKDQYHDWVKQEGIDRVLPDIVPTGQLYQVDLCGRKVDIGVGIHDSSSALASYL 241 T+LWDF K +YH+WVK E ID P + + G V +GVG+HDSS+AL YL Sbjct: 182 TQLWDFNKSEYHNWVKTEKIDEKFGTFTPADSSLKTNFEGSSVKVGVGLHDSSAALIPYL 241 Query: 242 VRVKEPFLLISTGTWSISLNPFTTDPLTKDELHNDCLNFLSIEGKPVKASRFFMGYEFNY 301 PF+LISTGTW ISLNPF +PLT +EL DCL ++ +GK VKASR F GYE Sbjct: 242 ANFNTPFVLISTGTWCISLNPFNQEPLTAEELKQDCLCYMHFKGKAVKASRIFAGYEHEV 301 Query: 302 QIDRINKHFGKPDKFYKSVPANPAIIKAIKTGKVSNTFYPRHIAETPLVKALYEGNEWNP 361 Q+ RI +HF + +K + NP++I K++N P + E A E + Sbjct: 302 QLKRIAEHFDRAAYLFKHLKFNPSMIL-----KLANKI-PENRQEQQGFSASSAFPERDL 355 Query: 362 ASFANFDEAYHHLIWGLTLLQVESLKLARGNSGIKKVFIDGGFVHNEVFMELLRYYLPES 421 F +EAYH LI+ L Q+ SLKL N+G+K++F+DGGF N ++M LL +P+ Sbjct: 356 NLFQTAEEAYHQLIFDLIKQQIYSLKLIL-NTGVKRIFVDGGFGKNAIYMHLLATSIPDI 414 Query: 422 ELEFSDFPLGSAYGAALVL 440 E+ S +A G AL + Sbjct: 415 EVYASSVSQATAIGTALAI 433 Lambda K H 0.319 0.138 0.418 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: 683 Number of extensions: 30 Number of successful extensions: 4 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: 448 Length of database: 461 Length adjustment: 33 Effective length of query: 415 Effective length of database: 428 Effective search space: 177620 Effective search space used: 177620 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 (21.7 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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