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: E9B1N7
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 | 285 | 289 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.663 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.397 |
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 | 476 | 480 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.395 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.317 |
DEG_SCF_FBW7_2 | 295 | 302 | PF00400 | 0.556 |
DOC_CDC14_PxL_1 | 325 | 333 | PF14671 | 0.513 |
DOC_CKS1_1 | 336 | 341 | PF01111 | 0.531 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.786 |
DOC_CYCLIN_RxL_1 | 49 | 58 | PF00134 | 0.458 |
DOC_MAPK_MEF2A_6 | 509 | 518 | PF00069 | 0.669 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.466 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.447 |
DOC_PP2B_LxvP_1 | 353 | 356 | PF13499 | 0.685 |
DOC_PP2B_LxvP_1 | 57 | 60 | PF13499 | 0.503 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.762 |
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 | 315 | 319 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.524 |
DOC_USP7_UBL2_3 | 461 | 465 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 594 | 598 | PF12436 | 0.573 |
DOC_USP7_UBL2_3 | 600 | 604 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.553 |
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 | 158 | 163 | PF00244 | 0.216 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 369 | 376 | PF00244 | 0.581 |
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 | 0.700 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.339 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.557 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.695 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.598 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.386 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.466 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.553 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.626 |
LIG_Integrin_RGD_1 | 431 | 433 | PF01839 | 0.647 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.347 |
LIG_MYND_1 | 329 | 333 | PF01753 | 0.695 |
LIG_PCNA_PIPBox_1 | 247 | 256 | PF02747 | 0.270 |
LIG_PCNA_yPIPBox_3 | 244 | 254 | PF02747 | 0.270 |
LIG_PCNA_yPIPBox_3 | 465 | 479 | PF02747 | 0.572 |
LIG_PTB_Apo_2 | 133 | 140 | PF02174 | 0.339 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.283 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.487 |
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 | 0.541 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.450 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.414 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.647 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.627 |
LIG_SH3_CIN85_PxpxPR_1 | 340 | 345 | PF14604 | 0.717 |
LIG_SUMO_SIM_anti_2 | 174 | 179 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 209 | 216 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.373 |
LIG_TRFH_1 | 376 | 380 | PF08558 | 0.689 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.339 |
LIG_TYR_ITIM | 277 | 282 | PF00017 | 0.465 |
LIG_WW_3 | 354 | 358 | PF00397 | 0.669 |
MOD_CAAXbox | 607 | 610 | PF01239 | 0.565 |
MOD_CDC14_SPxK_1 | 65 | 68 | PF00782 | 0.580 |
MOD_CDK_SPK_2 | 426 | 431 | PF00069 | 0.722 |
MOD_CDK_SPxK_1 | 62 | 68 | PF00069 | 0.556 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.350 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.425 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.335 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.792 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.767 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.562 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.518 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.706 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.563 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.480 |
MOD_Cter_Amidation | 482 | 485 | PF01082 | 0.606 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.391 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.456 |
MOD_GlcNHglycan | 223 | 227 | PF01048 | 0.402 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.329 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.339 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.606 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.581 |
MOD_GlcNHglycan | 405 | 409 | PF01048 | 0.711 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.586 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.684 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.733 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.414 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.239 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.269 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.354 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.615 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.636 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.647 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.804 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.395 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.730 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.639 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.460 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.440 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.196 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.339 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.316 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.606 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.410 |
MOD_N-GLC_2 | 606 | 608 | PF02516 | 0.614 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.573 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.326 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.557 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.588 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.740 |
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_PIKK_1 | 378 | 384 | PF00454 | 0.592 |
MOD_PK_1 | 55 | 61 | PF00069 | 0.571 |
MOD_PKA_1 | 357 | 363 | PF00069 | 0.543 |
MOD_PKA_1 | 596 | 602 | PF00069 | 0.620 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.610 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.622 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.564 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.754 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.422 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.334 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.563 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.396 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.662 |
MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.563 |
MOD_Plk_2-3 | 233 | 239 | PF00069 | 0.216 |
MOD_Plk_2-3 | 372 | 378 | PF00069 | 0.696 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.685 |
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 | 0.595 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.386 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.642 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.283 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.621 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.640 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.648 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.636 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.776 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.633 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.561 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.466 |
MOD_SUMO_rev_2 | 459 | 466 | PF00179 | 0.709 |
MOD_SUMO_rev_2 | 469 | 478 | PF00179 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 552 | 555 | PF00400 | 0.577 |
TRG_NLS_MonoExtC_3 | 198 | 203 | PF00514 | 0.399 |
TRG_NLS_MonoExtC_3 | 595 | 600 | PF00514 | 0.536 |
TRG_NLS_MonoExtN_4 | 196 | 203 | PF00514 | 0.317 |
TRG_NLS_MonoExtN_4 | 594 | 601 | PF00514 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTB6 | Leptomonas seymouri | 45% | 97% |
A0A3Q8IER9 | Leishmania donovani | 86% | 100% |
A4HJ62 | Leishmania braziliensis | 63% | 99% |
A4I6I0 | Leishmania infantum | 87% | 100% |
Q4Q6H7 | Leishmania major | 83% | 100% |