Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8INJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008017 | microtubule binding | 5 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.816 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.816 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.753 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.422 |
CLV_Separin_Metazoa | 386 | 390 | PF03568 | 0.572 |
CLV_Separin_Metazoa | 89 | 93 | PF03568 | 0.565 |
DEG_APCC_DBOX_1 | 115 | 123 | PF00400 | 0.469 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.617 |
DOC_CYCLIN_RxL_1 | 454 | 464 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 133 | 141 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 406 | 412 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 454 | 462 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 155 | 162 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 17 | 24 | PF00069 | 0.644 |
DOC_MAPK_MEF2A_6 | 174 | 183 | PF00069 | 0.303 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.675 |
DOC_USP7_UBL2_3 | 407 | 411 | PF12436 | 0.572 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 229 | 233 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 353 | 360 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.635 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.654 |
LIG_CaM_IQ_9 | 34 | 50 | PF13499 | 0.452 |
LIG_Clathr_ClatBox_1 | 159 | 163 | PF01394 | 0.577 |
LIG_EH1_1 | 396 | 404 | PF00400 | 0.549 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.567 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.556 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.580 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.610 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.637 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.590 |
LIG_GBD_Chelix_1 | 461 | 469 | PF00786 | 0.515 |
LIG_LIR_Apic_2 | 238 | 244 | PF02991 | 0.773 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.645 |
LIG_MAD2 | 280 | 288 | PF02301 | 0.762 |
LIG_NRBOX | 464 | 470 | PF00104 | 0.522 |
LIG_NRBOX | 86 | 92 | PF00104 | 0.531 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.649 |
LIG_SH2_NCK_1 | 267 | 271 | PF00017 | 0.674 |
LIG_SH2_SRC | 241 | 244 | PF00017 | 0.686 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.735 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.596 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.484 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.746 |
LIG_SH3_CIN85_PxpxPR_1 | 200 | 205 | PF14604 | 0.592 |
LIG_SUMO_SIM_anti_2 | 86 | 92 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.577 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.730 |
LIG_TRAF2_1 | 383 | 386 | PF00917 | 0.585 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.499 |
LIG_WW_3 | 242 | 246 | PF00397 | 0.684 |
MOD_CDC14_SPxK_1 | 336 | 339 | PF00782 | 0.739 |
MOD_CDK_SPxK_1 | 333 | 339 | PF00069 | 0.739 |
MOD_CDK_SPxxK_3 | 333 | 340 | PF00069 | 0.739 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.599 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.592 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.714 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.702 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.771 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.646 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.590 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.510 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.589 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.729 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.721 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.682 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.721 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.542 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.431 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.714 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.600 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.588 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.814 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.753 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.810 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.694 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.563 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.704 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.586 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.568 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.614 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.522 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.695 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.728 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.628 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.770 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.634 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.463 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.570 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.763 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.778 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.689 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.477 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.472 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.593 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.771 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.677 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.606 |
MOD_NEK2_2 | 294 | 299 | PF00069 | 0.727 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.635 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.588 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.811 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.582 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.717 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.600 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.630 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.467 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.666 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.529 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.727 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.607 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.780 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.487 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.708 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.712 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.758 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.722 |
MOD_SUMO_for_1 | 148 | 151 | PF00179 | 0.579 |
MOD_SUMO_for_1 | 165 | 168 | PF00179 | 0.435 |
MOD_SUMO_rev_2 | 128 | 137 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 21 | 30 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 408 | 413 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_1 | 464 | 469 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_4 | 96 | 102 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.654 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.814 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 411 | 415 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 466 | 471 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7F5 | Leptomonas seymouri | 58% | 98% |
A0A0S4ISW4 | Bodo saltans | 34% | 100% |
A0A1X0P856 | Trypanosomatidae | 40% | 100% |
A0A3R7RIJ2 | Trypanosoma rangeli | 38% | 100% |
A4HP16 | Leishmania braziliensis | 79% | 100% |
A4IDC6 | Leishmania infantum | 99% | 100% |
E9ASS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q1R9 | Leishmania major | 94% | 100% |
V5BU44 | Trypanosoma cruzi | 40% | 100% |