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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3S7X7H5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.500 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.506 |
CLV_Separin_Metazoa | 60 | 64 | PF03568 | 0.507 |
DEG_APCC_DBOX_1 | 331 | 339 | PF00400 | 0.528 |
DEG_APCC_KENBOX_2 | 310 | 314 | PF00400 | 0.583 |
DOC_CDC14_PxL_1 | 245 | 253 | PF14671 | 0.496 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.632 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 117 | 121 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.615 |
LIG_Actin_WH2_2 | 324 | 341 | PF00022 | 0.556 |
LIG_Actin_WH2_2 | 33 | 49 | PF00022 | 0.590 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.658 |
LIG_eIF4E_1 | 240 | 246 | PF01652 | 0.462 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.493 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.542 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.485 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.610 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.579 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.482 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.477 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.629 |
LIG_LIR_Apic_2 | 139 | 144 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 176 | 180 | PF02991 | 0.450 |
LIG_MYND_1 | 57 | 61 | PF01753 | 0.525 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.443 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.454 |
LIG_Rb_LxCxE_1 | 119 | 133 | PF01857 | 0.517 |
LIG_REV1ctd_RIR_1 | 181 | 191 | PF16727 | 0.454 |
LIG_SH2_GRB2like | 112 | 115 | PF00017 | 0.371 |
LIG_SH2_NCK_1 | 124 | 128 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.533 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.509 |
LIG_SH2_SRC | 124 | 127 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.457 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.544 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.428 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.590 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.710 |
LIG_SUMO_SIM_par_1 | 247 | 253 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 317 | 324 | PF11976 | 0.530 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.518 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.548 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.536 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.556 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.744 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.482 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.520 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.596 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.665 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.489 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.565 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.541 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.622 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.686 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.561 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.534 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.505 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.376 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.532 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.535 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.430 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.529 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.554 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.532 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.605 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.485 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.546 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.708 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.568 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.625 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.592 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.454 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.497 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.478 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.494 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.574 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.544 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.530 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.416 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.709 |
MOD_SUMO_rev_2 | 101 | 108 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 14 | 23 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 81 | 88 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.690 |
TRG_DiLeu_BaEn_3 | 132 | 138 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.493 |
TRG_NES_CRM1_1 | 147 | 161 | PF08389 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK09 | Leptomonas seymouri | 60% | 93% |
A0A0S4KNI9 | Bodo saltans | 21% | 100% |
A4HAF5 | Leishmania braziliensis | 74% | 100% |
A4I9L1 | Leishmania infantum | 100% | 100% |
E9B4K9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q3G7 | Leishmania major | 94% | 100% |
V5BHQ7 | Trypanosoma cruzi | 31% | 100% |