Align Inositol transport ATP-binding protein IatA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate WP_110805879.1 C8J30_RS10885 sugar ABC transporter ATP-binding protein
Query= TCDB::B8H229 (515 letters) >NCBI__GCF_003217355.1:WP_110805879.1 Length = 511 Score = 337 bits (865), Expect = 5e-97 Identities = 194/487 (39%), Positives = 291/487 (59%), Gaps = 5/487 (1%) Query: 11 KSFPGVRALDQVDLVVGVGEVHALLGENGAGKSTLIKILSAAHAADAGTVTFAGQVLDPR 70 K +PG RAL VD + +G V+ L+GENGAGKSTL+K+++ GT+T G+ + R Sbjct: 16 KVYPGTRALKGVDFDLRMGAVNVLVGENGAGKSTLMKLIAGVEDMTEGTITMDGREMRFR 75 Query: 71 DAPLRRQQLGIATIYQEFNLFPELSVAENMYLGREPRRLGL-VDWSRLRADAQALLNDLG 129 GI ++QE NLFP LSVAEN+++G E R G+ +D R + L+ L Sbjct: 76 -TKADAVAAGIGIVFQELNLFPNLSVAENIFIGHETTRGGIDIDIEAHREATRQLMERLE 134 Query: 130 LPLNPDAPVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREVDRLHAIIAGLKAR 189 ++PD P+ L + +QQ+VEIAKA+ NAR++I+DEPT+ALS EV+ L +I L A+ Sbjct: 135 QNIHPDTPLGNLRIGQQQIVEIAKALAQNARILILDEPTSALSAAEVEVLFRVIDELTAQ 194 Query: 190 SVSVIYVSHRLGEVKAMCDRYTVMRDGRFVASGDVADVEVADMVRLMVGRHVEFERRKRR 249 V ++Y+SHRL E+ + D TV+RDG + + V++ +V+ M+G + R Sbjct: 195 GVGIVYISHRLEELIRVGDYITVLRDGVITGARSMEGVDIPWIVKAMIGSSSKEYGRSEV 254 Query: 250 RPPGAVVLKVEGVTPAAPRLSAPGYLRQVSFAARGGEIVGLAGLVGAGRTDLARLIFGAD 309 G + + E +T PR + VS + R GEIVGL GL+GAGR++ + Sbjct: 255 ANFGPEIFRAEDIT--LPRAGGGFTVDHVSLSIRSGEIVGLYGLMGAGRSEFLECVMAQH 312 Query: 310 PIAAGRVLVDDKPLRLRSPRDAIQAGIMLVPEDRKQQGCFLDHSIRRNLSLPSLKALSAL 369 P + G+ V+ KPL R I GI L+PEDRK+ G SIR NL+L SL + + L Sbjct: 313 PHSGGKFWVEGKPLTERDVPGRIARGIALIPEDRKRDGLIQIMSIRENLTLSSLPSFTKL 372 Query: 370 GQWVDERAERDLVETYRQKLRIKMADAETAIGKLSGGNQQKVLLGRAMALTPKVLIVDEP 429 +D + E + ++L IK+A E + LSGGNQQKV++G+A+ PKVL++DEP Sbjct: 373 FH-LDLKKEAKTAVEFIKRLTIKVASPENPVSSLSGGNQQKVVIGKALMTGPKVLLMDEP 431 Query: 430 TRGIDIGAKAEVHQVLSDLADLGVAVVVISSELAEVMAVSDRIVVFREGVIVADLDAQTA 489 +RGIDIGAKAEV + + LA G+ ++ ++S+L EV+A+SDRI+V +G + + + T Sbjct: 432 SRGIDIGAKAEVFRTMRRLAAEGLGILFVTSDLDEVLALSDRIIVMAQGRVTGEFPSGTE 491 Query: 490 TEEGLMA 496 + + A Sbjct: 492 AAKVISA 498 Lambda K H 0.320 0.136 0.380 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: 634 Number of extensions: 34 Number of successful extensions: 9 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: 515 Length of database: 511 Length adjustment: 35 Effective length of query: 480 Effective length of database: 476 Effective search space: 228480 Effective search space used: 228480 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 Sep 24 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:
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