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. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HJ62
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0003924 | GTPase activity | 7 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005525 | GTP binding | 5 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 7 |
GO:0019001 | guanyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.235 |
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.445 |
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 536 | 540 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.744 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.546 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.396 |
CLV_PCSK_PC7_1 | 195 | 201 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.548 |
DEG_COP1_1 | 315 | 325 | PF00400 | 0.555 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.533 |
DEG_SCF_FBW7_1 | 428 | 434 | PF00400 | 0.567 |
DEG_SCF_TRCP1_1 | 77 | 82 | PF00400 | 0.521 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.555 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.793 |
DOC_MAPK_MEF2A_6 | 339 | 346 | PF00069 | 0.564 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.630 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.772 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.394 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.253 |
DOC_USP7_UBL2_3 | 593 | 597 | PF12436 | 0.571 |
DOC_USP7_UBL2_3 | 599 | 603 | PF12436 | 0.602 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.241 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 504 | 511 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 266 | 284 | PF00022 | 0.480 |
LIG_APCC_ABBA_1 | 250 | 255 | PF00400 | 0.343 |
LIG_BIR_III_4 | 414 | 418 | PF00653 | 0.590 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.343 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.343 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.338 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.583 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.580 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.510 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.574 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.387 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.561 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.480 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.549 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.272 |
LIG_LIR_Apic_2 | 324 | 328 | PF02991 | 0.739 |
LIG_LIR_Gen_1 | 248 | 258 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.353 |
LIG_PCNA_yPIPBox_3 | 466 | 480 | PF02747 | 0.567 |
LIG_PTB_Apo_2 | 133 | 140 | PF02174 | 0.343 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.288 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.253 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.284 |
LIG_SH2_NCK_1 | 258 | 262 | PF00017 | 0.343 |
LIG_SH2_SRC | 258 | 261 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.461 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.664 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.748 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.581 |
LIG_SUMO_SIM_anti_2 | 173 | 179 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.375 |
LIG_TYR_ITIM | 256 | 261 | PF00017 | 0.343 |
LIG_WRC_WIRS_1 | 322 | 327 | PF05994 | 0.546 |
MOD_CAAXbox | 606 | 609 | PF01239 | 0.591 |
MOD_CDC14_SPxK_1 | 224 | 227 | PF00782 | 0.253 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.253 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.266 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.430 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.248 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.429 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.347 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.526 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.564 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.641 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.767 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.599 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.549 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.681 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.652 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.556 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.272 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.623 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.542 |
MOD_Cter_Amidation | 591 | 594 | PF01082 | 0.461 |
MOD_DYRK1A_RPxSP_1 | 200 | 204 | PF00069 | 0.241 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.241 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.470 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.340 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.343 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.599 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.584 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.736 |
MOD_GlcNHglycan | 406 | 410 | PF01048 | 0.729 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.554 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.698 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.562 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.773 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.577 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.627 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.538 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.256 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.280 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.334 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.608 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.630 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.639 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.798 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.396 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.655 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.424 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.654 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.457 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.197 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.343 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.243 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.579 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.502 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.455 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.333 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.291 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.637 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.536 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.746 |
MOD_NEK2_2 | 109 | 114 | PF00069 | 0.343 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.565 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.574 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.479 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.406 |
MOD_PK_1 | 158 | 164 | PF00069 | 0.333 |
MOD_PK_1 | 55 | 61 | PF00069 | 0.553 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.253 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.253 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.696 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.557 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.539 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.565 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.769 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.350 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.556 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.299 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.253 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.436 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.684 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.397 |
MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.556 |
MOD_Plk_2-3 | 214 | 220 | PF00069 | 0.449 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.352 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.241 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.633 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.572 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.387 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.656 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.323 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.241 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.445 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.648 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.693 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.640 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.619 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.804 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.633 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.480 |
MOD_SUMO_rev_2 | 460 | 467 | PF00179 | 0.721 |
TRG_DiLeu_BaEn_1 | 475 | 480 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.285 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 579 | 583 | PF00026 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTB6 | Leptomonas seymouri | 46% | 97% |
A0A3Q8IER9 | Leishmania donovani | 64% | 100% |
A4I6I0 | Leishmania infantum | 64% | 100% |
E9B1N7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4Q6H7 | Leishmania major | 64% | 100% |