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: A4I6I0
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 | 220 | 224 | PF00656 | 0.433 |
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.747 |
CLV_C14_Caspase3-7 | 534 | 538 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.720 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.569 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.397 |
CLV_PCSK_PC7_1 | 196 | 202 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.317 |
DOC_CKS1_1 | 426 | 431 | PF01111 | 0.793 |
DOC_CYCLIN_RxL_1 | 49 | 58 | PF00134 | 0.456 |
DOC_MAPK_MEF2A_6 | 508 | 517 | PF00069 | 0.601 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.466 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.672 |
DOC_PP2B_LxvP_1 | 57 | 60 | PF13499 | 0.495 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.770 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.310 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.655 |
DOC_USP7_UBL2_3 | 460 | 464 | PF12436 | 0.652 |
DOC_USP7_UBL2_3 | 592 | 596 | PF12436 | 0.542 |
DOC_USP7_UBL2_3 | 597 | 601 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.613 |
LIG_Actin_WH2_2 | 181 | 198 | PF00022 | 0.317 |
LIG_Actin_WH2_2 | 267 | 285 | PF00022 | 0.466 |
LIG_APCC_ABBA_1 | 251 | 256 | PF00400 | 0.339 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.668 |
LIG_BIR_III_4 | 438 | 442 | PF00653 | 0.675 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.596 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.339 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.678 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.384 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.556 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.466 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.325 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.524 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.366 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.366 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.590 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.623 |
LIG_Integrin_RGD_1 | 430 | 432 | PF01839 | 0.645 |
LIG_LIR_Apic_2 | 325 | 329 | PF02991 | 0.738 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 571 | 580 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 571 | 576 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.347 |
LIG_MYND_1 | 329 | 333 | PF01753 | 0.705 |
LIG_PCNA_yPIPBox_3 | 464 | 478 | PF02747 | 0.547 |
LIG_PTB_Apo_2 | 133 | 140 | PF02174 | 0.339 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.339 |
LIG_SH2_SRC | 259 | 262 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.446 |
LIG_SH3_1 | 357 | 363 | PF00018 | 0.688 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.414 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.634 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.656 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.633 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.623 |
LIG_SH3_CIN85_PxpxPR_1 | 339 | 344 | PF14604 | 0.716 |
LIG_SUMO_SIM_anti_2 | 173 | 179 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 209 | 216 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.370 |
LIG_TRFH_1 | 375 | 379 | PF08558 | 0.695 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.339 |
LIG_TYR_ITIM | 277 | 282 | PF00017 | 0.471 |
LIG_WW_3 | 354 | 358 | PF00397 | 0.654 |
MOD_CAAXbox | 606 | 609 | PF01239 | 0.553 |
MOD_CDC14_SPxK_1 | 65 | 68 | PF00782 | 0.584 |
MOD_CDK_SPK_2 | 425 | 430 | PF00069 | 0.730 |
MOD_CDK_SPK_2 | 62 | 67 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 62 | 68 | PF00069 | 0.555 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.386 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.350 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.441 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.425 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.335 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.801 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.778 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.789 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.705 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.532 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.406 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.366 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.637 |
MOD_Cter_Amidation | 482 | 485 | PF01082 | 0.599 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.456 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.329 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.339 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.605 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.587 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.613 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.767 |
MOD_GlcNHglycan | 404 | 408 | PF01048 | 0.718 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.617 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.746 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.414 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.239 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.354 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.602 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.668 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.648 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.686 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.809 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.391 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.729 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.651 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.452 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.446 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.470 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.339 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.316 |
MOD_N-GLC_2 | 605 | 607 | PF02516 | 0.600 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.326 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.561 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.539 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.728 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.719 |
MOD_NEK2_2 | 109 | 114 | PF00069 | 0.339 |
MOD_NEK2_2 | 130 | 135 | PF00069 | 0.317 |
MOD_PK_1 | 158 | 164 | PF00069 | 0.328 |
MOD_PK_1 | 55 | 61 | PF00069 | 0.565 |
MOD_PKA_1 | 595 | 601 | PF00069 | 0.594 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.613 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.755 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.334 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.532 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.429 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.641 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.392 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.666 |
MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.532 |
MOD_Plk_2-3 | 215 | 221 | PF00069 | 0.433 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.707 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.684 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.333 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.317 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.383 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.536 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.384 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.656 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.433 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.644 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.645 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.723 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.633 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.791 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.639 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.559 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.466 |
MOD_SUMO_rev_2 | 458 | 465 | PF00179 | 0.710 |
MOD_SUMO_rev_2 | 468 | 477 | PF00179 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.495 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.564 |
TRG_NLS_MonoExtC_3 | 198 | 203 | PF00514 | 0.399 |
TRG_NLS_MonoExtC_3 | 591 | 596 | PF00514 | 0.496 |
TRG_NLS_MonoExtN_4 | 196 | 203 | PF00514 | 0.317 |
TRG_NLS_MonoExtN_4 | 590 | 596 | PF00514 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTB6 | Leptomonas seymouri | 47% | 97% |
A0A3Q8IER9 | Leishmania donovani | 99% | 100% |
A4HJ62 | Leishmania braziliensis | 64% | 99% |
E9B1N7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q6H7 | Leishmania major | 91% | 100% |