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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WQL0
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.673 |
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.711 |
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.607 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.344 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.511 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.689 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.666 |
DOC_CKS1_1 | 446 | 451 | PF01111 | 0.658 |
DOC_CYCLIN_RxL_1 | 342 | 352 | PF00134 | 0.552 |
DOC_CYCLIN_RxL_1 | 69 | 78 | PF00134 | 0.575 |
DOC_CYCLIN_RxL_1 | 87 | 95 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 130 | 139 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 368 | 375 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 173 | 180 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.569 |
DOC_MAPK_RevD_3 | 74 | 88 | PF00069 | 0.487 |
DOC_PP4_FxxP_1 | 57 | 60 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.651 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 219 | 224 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 368 | 376 | PF00244 | 0.408 |
LIG_BIR_III_2 | 114 | 118 | PF00653 | 0.545 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.660 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.540 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.573 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.448 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.516 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.648 |
LIG_Integrin_RGD_1 | 15 | 17 | PF01839 | 0.491 |
LIG_LIR_Apic_2 | 55 | 60 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 420 | 425 | PF02991 | 0.471 |
LIG_MAD2 | 135 | 143 | PF02301 | 0.503 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.498 |
LIG_PTAP_UEV_1 | 43 | 48 | PF05743 | 0.713 |
LIG_RPA_C_Plants | 248 | 259 | PF08784 | 0.554 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.483 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.522 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.712 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.659 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.378 |
LIG_TYR_ITSM | 418 | 425 | PF00017 | 0.567 |
LIG_UBA3_1 | 452 | 460 | PF00899 | 0.611 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.563 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.536 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.604 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.580 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.631 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.441 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.531 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.786 |
MOD_Cter_Amidation | 457 | 460 | PF01082 | 0.439 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.734 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.489 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.355 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.604 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.618 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.659 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.680 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.670 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.501 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.605 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.385 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.721 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.573 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.622 |
MOD_LATS_1 | 152 | 158 | PF00433 | 0.680 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.552 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.319 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.530 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.415 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.578 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.671 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.643 |
MOD_PK_1 | 219 | 225 | PF00069 | 0.728 |
MOD_PK_1 | 259 | 265 | PF00069 | 0.494 |
MOD_PKA_1 | 219 | 225 | PF00069 | 0.686 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.801 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.686 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.676 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.781 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.606 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.629 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.484 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.541 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.677 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.454 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.681 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.677 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.681 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.478 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.348 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.638 |
MOD_SUMO_for_1 | 378 | 381 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 352 | 358 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 94 | 99 | PF00179 | 0.510 |
TRG_DiLeu_BaEn_2 | 200 | 206 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 400 | 405 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.569 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.562 |
TRG_ER_diLys_1 | 459 | 462 | PF00400 | 0.604 |
TRG_NLS_Bipartite_1 | 281 | 301 | PF00514 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 403 | 407 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2N2 | Leptomonas seymouri | 56% | 98% |
A0A1X0NPB5 | Trypanosomatidae | 23% | 100% |
A0A3R7K7T1 | Trypanosoma rangeli | 32% | 100% |
A4H5L4 | Leishmania braziliensis | 77% | 100% |
A4HTV2 | Leishmania infantum | 99% | 78% |
D0A9B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AMP0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QHY6 | Leishmania major | 90% | 100% |